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Publications and Patents

ResearcherID:
L-9764-2015		ORCID:
0000-0002-2547-3037		Google Scholar profile

2024

251.
J. F. Goebel, F. Belitz, D. Sowa Prendes, Y. Haver, P. Diehl, M. Muhler, L. J Goossen, ChemSusChem 2024: Manganese Oxide / Silica catalysed Decarboxylative Ketonization of Aliphatic Carboxylic Acids in a Continuous Flow Reactor >>>DOI
250.
G. Heinrich, M. Kondratiuk, L. J. Gooßen & M. P. Wiesenfeldt, Nat Protoc 2024: Rapid reaction optimization by robust and economical quantitative benchtop 19F NMR spectroscopy >>>DOI
249.
Philipp J. Kohlpaintner, Niclas Schupp, Niklas Ehlenz, Lucas Marquart, Lukas J. Gooßen, and Siegfried R. Waldvogel, ACS Org. Lett. 2024: Synthesis of Aromatic N-Oxides Using Electrochemically Generated Peroxodicarbonate >>>DOI
248.
Fiona Sprang , Niclas Schupp , Philipp Kohlpaintner , Lukas J. Gooßen and Siegfried R Waldvogel, Green Chem. 2024, E-Dakin Reaction: Oxidation of Hydroxybenzaldehydes to Phenols with Electrochemically Generated Peroxodicarbonate as Sustainable Ex-Cell Oxidizer >>>DOI
247.
Svetlana A. Varenichenko , Victor Markov, Jonas F. Goebel, Oleg K. Farat, and Lukas J. Gooßen, J. Org. Chem. 2024, Vilsmeier−Haack-InitiatedFormylativeRearrangementofSpirodioxo-lan-5-onesinto Functionalized4,5,6,7-Tetrahydrobenzofurans >>>DOI
246.
Sourav Manna, Florian Papp, Yusei Hisata, Julian Löffler, Martyna Rybka, Viktoria Däschlein-Gessner, Yoichi Hoshimoto, Lukas J. Goossen, Adv. Synth. Catal.2024, Palladium-Catalyzed γ-Arylation of Acylketene Synthons with Aryl Chlorides Enabled by Ylide-Functionalized Phosphines (YPhos) >>>DOI;

2023

245.
Xianglin Luo, Zhewei Li, Yuzhen Zheng, Yueping Lin, Huanfeng Jiang, Lukas J. Gooßen, Ming Lei, and Liangbin Huang, ACS Catal. 2023, 13, 18, 12104–12113: Ligand-Enabled ortho-Arylation of (hetero)Aromatic Acids with 2,6-Disubstituted Aryl Halides >>>DOI
244.
D. Sowa Prendes, F. Papp, N. Sankaran, N. Sivendran, F. Beyer, C. Merten, L. J. Gooßen, Angew. Chem. 2023, e202309868: Enantioselektive Synthese von Arylglycinen durch Pd-katalysierte Kupplung von Schöllkopf-Bislactimethern mit Arylchloriden >>>DOI; Angew. Chem. Int. Ed. 2023, e202309868: Enantioselective Synthesis of Arylglycines via Pd-Catalyzed Coupling of Schöllkopf Bis-Lactim Ethers with Aryl Chlorides >>>DOI
243.
B. Xue, J. Shen, S. Manna, A. Doppiu, L. J. Goossen, Adv. Synth. Catal. 10.1002/adsc.202300761: Selective Monoarylation of Ammonium Triflate with Aryl Chlorides Catalyzed by [Pd(β-MeNAP)Br]2 and AdBrettPhos >>>DOI
242.
T. van Lingen, V. Bragoni, M. Dyga, B. Exner, D. Schick, C. Held, G. Sadowski, L. J. Gooßen, Angew. Chem. 2023, 135, e202303882: Salzabfall‑freie Carboxylierung von Acetylen: Grüne Synthese von C4‑Chemikalien durch einen CO2‑Druck‑induzierten Aciditätsswitch >>>DOI; Angew. Chem. Int. Ed. 2023, 62, e202210009: Carboxylation of Acetylene without Salt Waste: Green Synthesis of C4 Chemicals Enabled by a CO2-Pressure Induced Acidity Switch >>>DOI
241.
F. Papp, D. Sowa Prendes, S. Manna, A.-K. Seitz, S. Kostiukovska, J. Löffler, V. H. Gessner, L. J. Gooßen, ACS Catal. 2023, 13, 6846–6850: Palladium-Catalyzed Arylation of Hydantoins with Aryl Chlorides Enabled by Ylide-Functionalized Phosphines (YPhos) >>>DOI
240.
P. J. Kohlpaintner, L. Marquart, L. J. Gooßen, S. R. Waldvogel Eur. J. Org. Chem. 2023, e202300220: The Oxidation of Organo‐Boron Compounds Using Electrochemically Generated Peroxodicarbonate >>>DOI
239.
M. Kondratiuk, D. Gopinath, A. Elrrays, L. J. Gooßen, Eur. J. Lipid Sci. Technol. 2023, 125 , 2200163: Double-Bond Isomerization of Rapeseed Oil Methyl Esters in a Continuous Flow Reactor Efficiently Catalyzed by H-Mordenite >>>DOI
238.
J. F. Goebel, J. Löffler, Z. Zeng, J. Handelmann, A. Hermann, I. Rodstein, T. Gensch, V. H. Gessner, L. J. Goossen, Angew. Chem. 2023, 135, e2022161. Computergesteuerte Entwicklung von Ylid-funktionalisierten Phosphinen für Palladium-katalysierte Hiyama-Kupplungen >>>DOI; Angew. Chem. Int. Ed. 2023, 62, e202216160. Computer-Driven Development of Ylide Functionalized Phosphines for Palladium-Catalyzed Hiyama Couplings >>>DOI
237.
G. Bertoli, Á. M. Martínez, J. F. Goebel, D. Belmonte, N. Sivendran, L. J. Gooßen, Angew. Chem. 2023, 135, e202215. C−H-Fluormethoxylierung von Aromaten durch Photoredox-Katalyse >>>DOI; Angew. Chem. Int. Ed. 2023, 62, e202215920. C−H Fluoromethoxylation of Arenes by Photoredox Catalysis >>>DOI
236.
J. F. Goebel, J. Stemmer, F. Belitz, L. J. Goossen, Angew. Chem. 2023, e202301839. Mangan(I) katalysierte ortho C–H-Allylierung von Benzoesäuren >>>DOI; Angew. Chem. Int. Ed. 2023, e202301839, Manganese(I) Catalyzed ortho C–H Allylation of Benzoic Acids >>>DOI

2022

235.
D. Lichte, N. Pirkl, G. Heinrich, S. Dutta, J. F. Goebel, D. Koley, L. J. Gooßen, Angew. Chem. 2022, 134, e2022100: Palladium-katalysierte para-C−H Arylierung von Anilinen mit aromatischen Halogeniden >>>DOI; Angew. Chem. Int. Ed. 2022, e202210009: Palladium-Catalyzed para-C−H Arylation of Anilines with Aromatic Halides >>>DOI
234.
X.-J. Wei, B. Xue, J. Handelmann, Z. Hou, H. Dermandeh, V. H. Gessner, L. J. Goossen, Adv. Synt. Catal. 2022, 364, 19, 3336–3341: Ylide-Functionalized Diisopropyl Phosphine (prYPhos): A Ligand for Selective Suzuki-Miyaura Couplings of Aryl Chlorides >>DOI
233.
A.-K. Seitz, T. van Lingen, M. Dyga, P. J. Kohlpaintner, S. R. Waldvogel, L. Goossen, Synlett. 2022, 33, 15, 1527-1531 : Amine Oxidation by Electrochemically Generated Peroxodicarbonate. >>DOI
232.
F. Belitz , A.-K. Seitz, J. F. Goebel, Z. Hu, L. J. Goossen, Org. Lett. 2022, 24, 19, 3466–3470: Ru-Catalyzed C–H Arylation of Acrylic Acids with Aryl Bromides. >>DOI
231.
A.-K. Seitz, P. J. Kohlpaintner, T. van Lingen, M. Dyga, F. Sprang, M. Zirbes, S. R. Waldvogel, L. J. Goossen, Angew. Chem. 2022, 134, e2021175: Konzentriertes Wässriges Peroxodikarbonat: Effiziente Elektrosynthese und Anwendungen in Epoxidierungen, S-, und N-Oxidationen. >>>DOI; Angew. Chem. Int. Ed. 2022, 61, e202117563: Concentrated Aqueous Peroxodicarbonate: Efficient Electrosynthesis and Use as Oxidizer in Epoxidations, S-, and N-Oxidations. >>>DOI
230.
N. Sivendran, F. Belitz, D. Sowa Prendes, Á. M. Martínez, R. Schmid, L. J. Goossen, Chem. Eur. J. 2022, 28, e2021036: Photochemical Sandmeyer-type Halogenation of Arenediazonium Salts. >>>DOI
229.
J. F. Goebel, Z. Zeng, L. J. Gooßen, Synthesis 2022, 54, 565-569: Biaryl Synthesis via Electrooxidative Transition Metal Catalyzed C−H Activation. >>DOI

2021

228.
N. Sivendran, N. Pirkl, Z. Hu, A. Doppiu, L. J. Gooßen, Angew. Chem. 2021, 133, 25355-25364: Halogen-verbrückte Methylnaphthylpalladium-Dimere als vielseitig einsetzbare Katalysatorvorstufen in Kreuzkupplungen. >>>DOI; Angew. Chem. Int. Ed. 2021, 68, 25151-25160: Halogen-bridged Methylnaphthyl Palladium Dimers as Versatile Catalyst Precursors in Coupling Reactions. >>>DOI
227.
D. Koley, S. De, N. Sivendran, L. J. Gooßen, Chem. Eur. J. 2021, 15227-15239: Isomerization of Functionalized Olefins Using the Dinuclear Catalyst [PdI(μ-Br)(PtBu3)]2: A Mechanistic Study. >>DOI
226.
M. Dyga, C. Oppel, L. J. Gooßen, HardwareX 2021, 10, e00211: RotoMate: An open-source, 3D printed autosampler for use with benchtop nuclear magnetic resonance spectrometers. >>DOI
225.
Z. Zeng, J. F. Goebel, X. Liu, L. J. Gooßen, ACS Catal. 2021, 11, 11, 6626-6632: 2,2′-Biaryldicarboxylate Synthesis via Electrocatalytic Dehydrogenative C–H/C–H Coupling of Benzoic Acids. >>DOI
224.
Z. Hu, F. Belitz, G. Zhang, F. Papp, L. J. Gooßen, Org. Lett. 2021, 23, 9, 3541-3545: Ru-Catalyzed (E)-Specific ortho-C–H Alkenylation of Arenecarboxylic Acids by Coupling with Alkenyl Bromides. >>DOI
223.
Z. Zeng, A. Feceu, N. Sivendran, L. J. Gooßen, Adv. Synth. Catal. 2021, 363, 11, 2678-2722: Decarboxylation‐Initiated Intermolecular Carbon−Heteroatom Bond Formation. >>DOI
222.
E. Feresin, M. Kondratiuk, J. Nowack, L. J. Gooßen, Chemie in unserer Zeit, 2021, 55, 1, 28-37: Handreinigung auf molekularer Ebene – Die Rolle der Solvatation. >>DOI
221.
Z. Hu, X.-J. Wei, J. Handelmann, A.-K. Seitz, I. Rodstein, V. H. Gessner, L. J. Gooßen, Angew. Chem. 2021, 133, 6852-6858: Kupplung von Reformatsky-Reagenzien und Arylchloriden ermöglicht durch Ylid-funktionalisierte Phosphanliganden. >>>DOI; Angew. Chem. Int. Ed. 2021, 60, 12, 6778-6783: Coupling of Reformatsky Reagents with Aryl Chlorides enabled by Ylide‐Functionalized Phosphine Ligands. >>>DOI
220.
M. Ošeka, G. Laudadio, N. P. van Leest, M. Dyga, A. de A. Bartolomeu, L. J. Gooßen, B. de Bruin, K. T. de Oliveira, T. Noël, Chem 2021, 7, 1, 255-266: Electrochemical Aziridination of Internal Alkenes with Primary Amines. >>DOI

2020

219.
M. Dyga, F. Rudolphi, L. J. Gooßen, Nachrichten aus der Chemie 2020, 68, 27-28: Fair teilen. >>DOI
218.
Á. M. Martínez, D. Hayrapetyan, T. van Lingen, M. Dyga, L. J. Gooßen, Nat. Commun. 2020, 11, 4407: Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy. >>DOI
217.
S. De, N. Sivendran, B. Maity, N. Pirkl, D. Koley, L. J. Gooßen, ACS Catal. 2020, 10, 8, 4517-4533: Dinuclear PdI Catalysts in Equilibrium Isomerizations: Mechanistic Understanding, in Silico Casting, and Catalyst Development. >>DOI

2019

216.
X.-Q. Hu, D. Lichte, I. Rodstein, P. Weber, A.-K. Seitz, T. Scherpf, V. H. Gessner, L. J. Gooßen, Org. Lett. 2019, 21, 18, 7558–7562: Ylide-Functionalized Phosphine (YPhos)–Palladium Catalysts: Selective Monoarylation of Alkyl Ketones with Aryl Chlorides. >>DOI
215.
Z. Hu, X.-Q. Hu, G. Zhang, L. J. Gooßen, Org. Lett. 2019, 21, 17, 6770–6773: Ring-Opening Ortho-C–H Allylation of Benzoic Acids with Vinylcyclopropanes: Merging Catalytic C–H and C–C Activation Concepts. >>DOI
214.
G. Zhang, Z. Hu, G. Bertoli, L. J. Gooßen, ACS Catal. 2019, 9, 8153-8158: Iridium-Catalyzed Synthesis of Substituted Indanones from Aromatic Carboxylates and Unsaturated Ketones. >>DOI
213.
P. Weber, A. Biafora, A. Doppiu, H.-J. Bongard, H. Kelm, L. J. Gooßen, Org. Process Res. Dev. 2019, 23, 1462-1470: A comparative study of dibenzylideneacetone palladium complexes in catalysis. >>DOI
212.
P. Weber, C. K. Rank, E. Yalcinkaya, M. Dyga, T. van Lingen, R. Schmid, F. W. Patureau, L. J. Goossen, Adv. Synth. Catal. 2019, 361, 3925-3929: Rhodium-catalyzed ortho-Arylation of (Hetero)aromatic Acids. >>DOI
211.
M. S. Andrä, L. Schifferer, C. Pollok, C. Merten, L. J. Goossen, J-Q. Yu, Chem. Eur. J. 2019, 25, 8503-8507: Enantio‐ and Diastereoswitchable C‐H Arylation of Methylene Groups in Cycloalkanes. >>DOI
210.
Y. Gao, Y. Ou, L. J. Goossen, Chem. Eur. J. 2019, 25, 8709-8712: Pd‐Catalyzed Synthesis of Vinyl Arenes from Aryl Halides and Acrylic Acid. >>DOI
209.
N. Pirkl, A. Del Grosso, B. Mallick, A. Doppiu, L. J. Gooßen, Chem. Commun. 2019, 55, 5275-5278: Dihalogen-bridged NHC-palladium(I) dimers: synthesis, characterisation and applications in cross-coupling reactions. >>DOI
208.
M. Dyga, D. Hayrapetyan, R. K. Rit, L. J. Gooßen, Adv. Synth. Catal. 2019, 361, 3548-3553: Electrochemical ipso‐Thiocyanation of Arylboron Compounds. >>DOI
207.
G. Zhang, Z. Hu, F. Belitz, Y. Ou, N. Pirkl, L. J. Gooßen, Angew. Chem. 2019, 131, 6501-6505: Rhodium‐katalysierte Anellierung von Benzoesäuren mit α,β‐ungesättigten Ketonen durch C‐H‐, CO‐OH‐ und C‐C‐ Bindungsspaltung. >>DOI; Angew. Chem. Int. Ed. 2019, 58, 6435-6439: Rhodium‐Catalyzed Annelation of Benzoic Acids with α,β‐Unsaturated Ketones with Cleavage of C–H, CO–OH, and C–C Bonds. >>DOI
206.
J. Pollini, W. M. Pankau, L. J. Gooßen, Chem. Eur. J. 2019, 25, 7416-7425: Isomerizing Olefin Metathesis. >>DOI
205.
M. Pichette Drapeau, J. Bahri, D. Lichte, L. J. Gooßen, Angew. Chem. 2019, 131, 902-906: Decarboxylative ipso‐Amination of Activated Benzoic Acids. >>DOI; Angew. Chem. Int. Ed. 2019, 58, 892-896: Decarboxylative ipso‐Amination of Activated Benzoic Acids. >>DOI
204.
P. Weber, T. Scherpf, I. Rodstein, D. Lichte, L. T. Scharf, L. J. Gooßen, V. H. Gessner, Angew. Chem. 2019, 131, 3235-3239: Ein hochaktives, Ylid‐funktionalisiertes Phosphan für die palladiumkatalysierte Aminierung von Arylchloriden. >>DOI; Angew. Chem. Int. Ed. 2019, 58, 3203-3207: A Highly Active Ylide‐Functionalized Phosphine for Palladium‐Catalyzed Aminations of Aryl Chlorides. >>DOI

2018

203.
J. Pollini, V. Bragoni, L. J. Gooßen, Beilstein J. Org. Chem. 2018, 14, 2737-2744: Synthesis of a tyrosinase inhibitor by consecutive ethenolysis and cross-metathesis of crude cashew nutshell liquid. >>DOI
202.
Y. Ou, L. J. Gooßen, Asian J. Org. Chem. 2018, 8, 650-653: Copper-Mediated Synthesis of (Diethylphosphono)difluoromethyl Thioethers from Diazonium Salts, NaSCN, and TMS-CF2PO(OEt)2. >>DOI
201.
X.-Q. Hu, Z. Hu, G. Zhang, N. Sivendran, L. J. Gooßen, Org. Lett. 2018, 20, 4337-4340: Catalytic C−N and C−H Bond Activation: ortho-Allylation of Benzoic Acids with Allyl Amines. >>DOI
200.
V. Bragoni, R. K. Rit, R. Kirchmann, A. S. Trita and L. J. Gooßen, Green Chem. 2018, 20, 3210-3213: Synthesis of bio-based surfactants from cashew nutshell liquid in water. >>DOI
199.
D. Hayrapetyan, R. K. Rit, M. Kratz, K. Tschulik, L. J. Gooßen, Chem. Eur. J. 2018, 24, 11288-11291: Electrochemical C‐H Cyanation of Electron‐Rich (Hetero)Arenes. >>DOI
198.
X.-Q. Hu, Z. Hu, A. S. Trita, G. Zhang, L. J. Gooßen, Chem. Sci. 2018, 9, 5289-5294: Carboxylate-directed C–H allylation with Allyl alcohols or ethers. >>DOI
197.
H. Li, Q. Jiang, X. Jie, Y. Shang, Y. Zhang, L. J. Goossen, W. Su, ACS Catal. 2018, 8, 4777-4782: Rh/Cu-Catalyzed Ketone β‑Functionalization by Merging Ketone Dehydrogenation and Carboxyl-Directed C-H Alkylation. >>DOI
196.
G. Bertoli, B. Exner, M. V. Evers, K. Tschulik, L. J. Goossen, J. Fluor. Chem. 2018, 210, 132-136: Metal-free trifluoromethylthiolation of arenediazonium salts with Me4NSCF3. >>DOI
195.
T. Wendling, E. Risto, T. Krause, L. J. Goossen, Chem. Eur. J. 2018, 24, 6019-6024: Salt-Free Strategy for the Insertion of CO2 into C-H Bonds: Catalytic Hydroxymethylation of Alkynes. >>DOI
194.
G. Zhang, F. Jia, L. J. Goossen, Chem. Eur. J. 2018, 24, 4537-4541: Regioselective C–H Alkylation via Carboxylate-Directed Hydroarylation in Water. >>DOI
193.
S. Kovacs, B. Bayarmagnai, A. Aillerie, L. J. Goossen, Adv. Synth. Catal. 2018, 360, 1913-1918: Practical Reagents and Methods for Nucleophilic and Electrophilic Phosphorothiolations. >>DOI
192.
A. S. Trita, A. Biafora, M. Pichette-Drapeau, P. Weber, L. J. Goossen, Angew. Chem. 2018, 130, 14788-14792: Regiospecific ortho-C-H Allylation of Benzoic Acids. >>DOI; Angew. Chem. Int. Ed. 2018, 57, 14580-14584: Regiospecific ortho-C-H Allylation of Benzoic Acids.>>DOI
191.
L. J. Goossen, K. F. Pfister, S. Baader, patent WO 2017158060A1, 2017: Biofuel and method for a preparation by isomerizing metathesis.
 

2017


190.
K. F. Pfister, S. Baader, M. Baader, S. Berndt, L. J. Goossen, Sci. Adv. 2017, 3: Biofuel by isomerizing metathesis of rapeseed oil esters with (bio)ethylene for use in contemporary diesel engines. >>DOI

189.
A. Biafora, L. J. Goossen, Synlett 2017, 28, 1885-1890: Thieme Chemistry Journals Awardees – Where Are They Now? New Reaction Mode in Carboxylate-Directed C–H Functionalizations: Carboxylates as Deciduous Directing Groups. >>DOI

188.
L. J. Goossen, patent WO 2017093427, 2017: A process for preparing 1,4-butanediol from acethylene and carbon dioxide.

187.
D. Hackenberger, P. Weber, D. C. Blakemore, L. J. Goossen, J. Org. Chem. 2017, 82, 3917-3925: Synthesis of 3-Substituted 2-Arylpyridines via Cu/Pd-Catalyzed Decarboxylative Cross-Coupling of Picolinic Acids with (Hetero)Aryl Halides. >>DOI

186.
A. S. Trita, L. C. Over, J. Pollini, S. Baader, S. Riegsinger, M. A. R. Meier, L. J. Goossen, Green Chem. 2017, 19, 3051-3060: Synthesis of potential bisphenol A substitutes by isomerising metathesis of renewable raw materials. >>DOI

185.
A. Biafora, B. A. Khan, J. Bahri, J. M. Hewer, L. J. Goossen, Org. Lett. 2017, 19, 1232–1235: Doubly Regioselective C–H Hydroarylation of Unsymmetrical Alkynes Using Carboxylates as Deciduous Directing Groups. >>DOI

184.
S. Kovács, B. Bayarmagnai, L. J. Goossen, Adv. Synth. Catal. 2017, 359, 250-254: Preparation of Electrophilic Trifluoromethylthio Reagents from Nucleophilic Tetramethylammonium Trifluoromethylthiolate. >>DOI

183.
T. Wendling, E. Risto, B. Erb, L. J. Gooßen, Green Chem. 2017, 19, 643-646: Alkoxide-Catalyzed Addition of Alkyl Carbonates across Alkynes – Stereoselective Synthesis of (E)-β-Alkoxyacrylates. >>DOI

182.
L. J. Goossen, M. Grünberg, patent WO 2017093427, 2017: Arylation method.

181.
B. Exner, B. Bayarmagnai, C. Matheis, L. J. Goossen, J. Fluor. Chem. 2017, 198, 89-93: A Synthesis of perfluoroalkyl thioethers from aromatic thiocyanates by iron-catalysed decarboxylative perfluoroalkylation.>>DOI

2016


180.
A. Biafora, T. Krause, D. Hackenberger, F. Belitz, L. J. Gooßen, Angew. Chem. 2016, 128, 14972–14975: ortho-C–H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium; >>DOI
Angew. Chem. Int. Ed. 2016, 55, 14752–14755: ortho-C–H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium.
>>DOI

179.
M. Pichette Drapeau, L. J. Gooßen, Chem. Eur. J. 2016, 22, 18654: Carboxylic Acids as Directing Groups for C−H Bond Functionalization. (Minireview) >>DOI

178.
J. Tang, D. Hackenberger, L. J. Gooßen, Angew. Chem. 2016, 128, 11466-11470: Verzweigte Arylalkene aus Zimtsäuren: Selektivitätsumkehr in Heck-Reaktionen durch Carboxylate als abfallende dirigierende Gruppen. >>DOI; Angew. Chem. Int. Ed. 2016, 55, 11296-11299: Branched Arylalkenes from Cinnamates: Selectivity Inversion in Heck Reactions by Carboxylates as Deciduous Directing Groups. >>DOI

177.
C. Matheis, T. Krause, V. Bragoni, L. J. Gooßen, Chem. Eur. J. 2016, 22, 12270-12273: Trifluoromethylthiolation and Trifluoromethylselenolation of α-Diazo Esters Catalyzed by Copper. >>DOI

176.
C. Matheis, B. Bayarmagnai, K. Jouvin, L. J. Gooßen, Org. Chem. Front. 2016, 3, 949-952: Convenient Synthesis of Pentafluoroethyl Thioethers via Catalytic Sandmeyer Reaction with a Stable Fluoroalkylthiolation Reagent. >>DOI

175.
B. Erb, E. Risto, T. Wendling, L. J. Gooßen, ChemSusChem 2016, 9, 1442-1448: Reductive Etherification of Fatty Acids or Esters with Alcohols using Molecular Hydrogen. >>DOI

174.
T. Krause, S. Baader, B. Erb, L. J. Gooßen, Nat. Commun. 2016, 7, 11732: Atom-economic catalytic amide synthesis from amines and carboxylic acids activated in situ with acetylenes. >>DOI

173.
M. F. Grünberg, F. Jia, A. Rivas-Nass, L. J. Gooßen, Adv. Synth. Catal. 2016, 358, 1589-1594: Selective Monoarylation of Primary Anilines Catalyzed by Pd(dippf) and its Application in OLED Component Synthesis. >>DOI

172.
L. Huang, A. Biafora, G. Zhang, V. Bragoni, L. J. Gooßen, Angew. Chem. 2016, 128, 7047-7051: Regioselective C−H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups. >>DOI; Angew. Chem. Int. Ed. 2016, 55, 6933-6937: Regioselective C−H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups. >>DOI

171.
C. Matheis, V. Wagner, L. J. Gooßen, Chem. Eur. J. 2016, 22, 79-82 (hot paper): Sandmeyer-Type Trifluoromethylthiolation and Trifluoromethylselenolation of (Hetero)Aromatic Amines Catalyzed by Copper. >>DOI ( Cover >>DOI and Cover Profile >>DOI )

170.
B. Erb, M. Dierker, D. M. Ohlmann, L. J. Gooßen, Eur. J. Lipid. Sci. Tech. 2016, 118, 111-116 : Selective Synthesis of Propenyl-Branched Diunsaturated Fatty Esters via Catalytic Codimerization of Ethyl Linoleate and Propylene. >>DOI

2015


169.
B. Exner, B. Bayarmagnai, F. Jia, L. J. Gooßen, Chem. Eur. J. 2015, 21, 17220-17223: Iron-Catalyzed Decarboxylation of Trifluoroacetate and its Application to the Synthesis of Trifluoromethyl Thioethers. >>DOI

168.
D. Katayev, D. Hackenberger, L. J. Gooßen, The Catalyst Review 2015, 28, 6-11: Decarboxylative and Decarbonylative Reactions: An Industrial Perspective.

167.
D. Hackenberger, B. Song, M. F. Grünberg, S. Farsadpour, F. Menges, H. Kelm, C. Groß, T. Wolff, G. Niedner-Schatteburg, W. R. Thiel, L. J. Gooßen, ChemCatChem 2015, 7, 3579-3588: Bimetallic Cu/Pd Catalysts with Bridging Aminopyrimidinyl Phosphines for Decarboxylative Cross-Couplings at Moderate Temperatures. >>DOI

166.
L. Huang, D. Hackenberger, L. J. Gooßen, Angew. Chem. 2015, 127, 12798-12802: Iridium-katalysierte ortho-Arylierung von Benzoesäuren mit Aryldiazoniumsalzen. >>DOI; Angew. Chem. Int. Ed. 2015, 54, 12607-12611: Iridium-Catalyzed ortho-Arylation of Benzoic Acids with Arenediazonium Salts. >>DOI

165.
J. Tang, A. Biafora, L. J. Gooßen, Angew. Chem. 2015, 127, 13324-13327: Katalytische decarboxylierende Kreuzkupplung von Arylchloriden mit Benzoaten ohne aktivierende ortho-Substituenten. >>DOI; Angew. Chem. Int. Ed. 2015, 54, 13130-13133: Catalytic Decarboxylative Cross-Coupling of Aryl Chlorides and Benzoates without Activating ortho Substituents. >>DOI

164.
K. Jouvin, C. Matheis, L. J. Gooßen, Chem. Eur. J. 2015, 21, 14324-14327 (hot paper): Synthesis of Aryl Tri- and Difluoromethyl Thioethers via a C-H-Thiocyanation/Fluoroalkylation Cascade. >>DOI

163.
M. F. Grünberg, L. J. Gooßen, WO 2015059049 A1, 2015, Monoarylation of aromatic amines.

162.
C. Matheis, M. Wang, T. Krause, L. J. Gooßen, Synlett 2015, 26, 1628-1632: Metal-Free Trifluoromethylthiolation of Alkyl Electrophiles via a Cascade of Thiocyanation and Nucleophilic Cyanide–CF­3­ Substitution. >>DOI (Highlighted in Synform, 2015, 09, A122-A124. >>DOI)

161.
D. Katayev, B. Exner, L. J. Gooßen, ChemCatChem 2015, 7, 2028-2032: Synthesis of Biaryls by Decarboxylative Hiyama Coupling. >>DOI

160.
L. Huang, M. Arndt, K. Gooßen, H. Heydt, L. J. Gooßen, Chem. Rev. 2015, 115, 2596-2697: Late Transition Metal-Catalyzed Hydroamination and Hydroamidation. >>DOI

159.
B. Maity, L. J. Gooßen, D. Koley, Chem. Sci. 2015, 6, 2532-2552: Computational Study of the Mechanism and Selectivity of Ruthenium-Catalyzed Hydroamidations of Terminal Alkynes. >>DOI

158.
B. Bayarmagnai, C. Matheis, K. Jouvin, L. J. Gooßen, Angew. Chem. 2015, 127, 5845-5848: Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated in situ. >>DOI; Angew. Chem. Int. Ed. 2015, 54, 5753-5756: Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated in situ. >>DOI

2014


157.
C. Matheis, K. Jouvin, L. J. Gooßen, Org. Lett. 2014, 16, 5984-5987: Sandmeyer Difluoromethylation of (Hetero-)Arenediazonium Salts. >>DOI(Highlighted in Synfacts 2015, 11, 187. >>DOI)

156.
F. W. Patureau, L. J. Gooßen, Angew. Chem. 2014, 126, 5846-5847: Copper-Mediated Cross-Coupling Reactions. (book review) >>DOI; Angew. Chem. Int. Ed. 2014, 53, 5738-5739: Copper-Mediated Cross-Coupling Reactions. (book review) >>DOI

155.
K. F. Pfister, M. F. Grünberg, L. J. Gooßen, Adv. Synth. Catal. 2014, 356, 3302-3306: Synthesis of Allylarenes via Catalytic Decarboxylation of Allyl Benzoates. >>DOI

154.
S. Baader, P. E. Podsiadly, D. J. Cole-Hamilton, L. J. Gooßen, Green Chem. 2014, 16, 4885-4890: Synthesis of Tsetse Fly Attractants from a Cashew Nut Shell Extract by Isomerising Metathesis. >>DOI

153.
G. Danoun, B. Bayarmagnai, M. F. Grünberg, C. Matheis, E. Risto, L. J. Gooßen, Synthesis 2014, 46, 2283-2286: Sandmeyer Trifluoromethylation. >>DOI

152.
A. Fromm, C. van Wüllen, D. Hackenberger, L. J. Gooßen, J. Am. Chem. Soc. 2014, 136, 10007-10023: Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation. >>DOI

151.
D. Katayev, K. F. Pfister, T. Wendling, L. J. Gooßen, Chem. Eur. J. 2014, 20, 9902-9905: Copper-Mediated ortho-Nitration of (Hetero)Arenecarboxylates. >>DOI (Highlighted in Synfacts 2014, 10, 1198.>>DOI

150.
B. Bayarmagnai, C. Matheis, E. Risto, L. J. Gooßen, Adv. Synth. Catal. 2014, 356, 2343-2348: One-Pot Sandmeyer Trifluoromethylation and Trifluoromethylthiolation. >>DOI

149.
J. Tang, L. J. Gooßen, Org. Lett. 2014, 16, 2664-2667: Arylalkene Synthesis via Decarboxylative Cross-Coupling of Alkenyl Halides. >>DOI

148.
G. Danoun, B. Bayarmagnai, M. F. Grünberg, L. J. Gooßen, Chem.Sci. 2014, 5, 1312-1316: Sandmeyer Trifluormethylthiolation of Arenediazoniumsalts with Sodium Thiocyanate and Ruppert-Prakash Reagent. >>DOI

147.
L. J. Gooßen, P. Mamone, G. Danoun, A. Cotte, WO 2014167017 , 2014: Method for preparation of ortho-​acylated (hetero)​aromatic carboxylic acids.

146.
L. J. Gooßen, M. Arndt, WO 2014029689, 2014: Method for producing acetylenedicarboxylic acid from acetylene and carbon dioxide.

145.
L. J. Gooßen, M. Arndt, P. Mamone, M. Grünberg, US 20140187803, 2014: Method for the preparation of palladium(I) tri-​tert-​butylphosphine bromide dimer and process for its use in isomerization reactions.

144.
L. J. Gooßen, F. Rudolphi, B. Song, A. Cotte, M. Cotta, US 20140100371 , 2014: Process for preparing azomethines from alpha-​oxocarboxylates, amines and aryl bromides.

143.
L. J. Gooßen, T. Knauber, B. Song, A. Cotte, J. Mohr, WO 2014111493, 2014: Substituted benzimidazole phosphine compounds as ligands for palladium​/copper-​catalyzed decarboxylative coupling of aryl sulfonates with arenecarboxylic derivatives into biaryls.

142.
L. J. Gooßen, D. Ohlmann, M. Dierker, WO 2014001101, 2014: Method for producing unsaturated compounds.

2013


141.
L. J. Gooßen, D. Ohlmann, M. Dierker, US 20130340327, 2013: Process for preparing unsaturated compounds.

140.
G. Danoun, P. Mamone, L. J. Gooßen, Chem. Eur. J. 2013, 19, 17287-17290: One Pot-Synthesis of 3-Alkylidenephthalides from Benzoic Acids via a Rhodium-Catalyzed ortho-C-H Acylation Process. >>DOI

139.
S. Bhadra, W. Dzik, L. J. Gooßen, Synthesis 2013, 45, 2387-2390: Synthesis of Aryl Ethers from Aromatic Carboxylic Acids. >>DOI

138.
G. Danoun, B. Bayarmagnai, M. F. Grünberg, L. J. Gooßen, Angew. Chem 2013, 125, 8130-8133: Sandmeyer-Trifluormethylierung von Aryldiazoniumtetrafluorboraten. >>DOI; Angew. Chem. Int. Ed. 2013, 52, 7972-7975 (hot paper): Sandmeyer Trifluoromethylation of Arenediazonium Tetrafluoroborates. >>DOI

137.
S. Bhadra, C. Matheis, D. Katayev, L. J. Gooßen, Angew. Chem 2013, 125, 9449-9453: Copper-Catalyzed Dehydrogenative Coupling of Arenes and Alcohols. >>DOI; Angew. Chem. Int. Ed. 2013, 52, 9279-9283 (hot paper): Copper-Catalyzed Dehydrogenative Coupling of Arenes and Alcohols. >>DOI

136.
M. F. Grünberg, L. J. Gooßen J. Organomet. Chem. 2013, 744, 140-143: Decarboxylative Allylation of Arylglyoxylic Acids with Allyl Alcohol. >>DOI

135.
S. Baader, D. Ohlmann, L. J. Gooßen, Chem. Eur. J. 2013, 19, 9807-9810: Isomerizing ethenolysis as an efficient strategy for styrene synthesis. >>DOI

134.
M. F. Grünberg, L. J. Gooßen, Chem. Eur. J. 2013, 19, 7334-7337: Synthesis of Arylacetates from Benzylic Alcohols and Oxalate Esters via Decarboxylative Coupling. >>DOI

133.
P. Mamone, G. Danoun, L. J. Gooßen, Angew. Chem 2013, 125, 6836-6840: Rhodium-Catalyzed ortho Acylation of Aromatic Carboxylic Acids. >>DOI; Angew. Chem. Int. Ed. 2013, 52, 6704-6708: Rhodium-Catalyzed ortho Acylation of Aromatic Carboxylic Acids. >>DOI

132.
K. S. M. Salih, P. Mamone, G. Dörr, T. O. Bauer, A. Brodyanski, C. Wagner, M. Kopnarski, R. N. Klupp Taylor, S. Demeshko, F. Mayer, V. Schünemann, S. Ernst, L. J. Gooßen, W. R. Thiel, Chem. Mater. 2013, 25, 1430-1435: Facile Synthesis of Monodisperse Maghemite and Ferrite Nanocrystals from Metal Powder and Octanoic Acid. >>DOI

131.
S. Bhadra, W. Dzik, L. J. Gooßen, Angew. Chem 2013, 125, 3031-3035: Synthese von Arylethern aus Benzoaten über carboxylatdirigierte C-H-aktivierende Alkoxylierung mit gekoppelter Protodecarboxylierung. >>DOI; Angew. Chem. Int. Ed. 2013, 52, 2959-2962 (hot paper): Synthesis of Aryl Ethers from Benzoates via Carboxylate-Directed C-H Activating Alkoxylation with Concomitant Protodecarboxylation. >>DOI

130.
B. Song, T. Knauber, L. J. Gooßen, Angew. Chem 2013, 125, 3026-3030: Decarboxylierende Kreuzkupplung von Mesylaten katalysiert durch ein Kupfer/Palladium-System mit maßgeschneiderten Imidazolylphosphanliganden. >>DOI; Angew. Chem. Int. Ed. 2013, 52, 2954-2958: Decarboxylative Cross-Coupling of Mesylates Catalyzed by Copper/Palladium Systems with Customized Imidazolyl Phosphine Ligands. >>DOI

129.
L. J. Gooßen, P. Mamone, in Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook, 3rd ed. (Eds.: B. Cornils, W. A. Herrmann, M. Beller), 2013, Decarbonylative and Decarboxylative Processes.

128.
L. J. Gooßen, K. Gooßen in Top. Organomet. Chem.: Inventing Reactions (Ed.: L. J. Gooßen), Springer, Berlin-Heidelberg,2013, 44, 121-141: Decarboxylative Coupling Reactions. >>DOI

127.
L. J. Gooßen, M. Arndt, P. Mamone, M. F. Grünberg, WO 2013000874, 2013: Method for the preparation of Palladium(l) tri-tert-butylphosphine bromide dimer and process for its use in isomerization reactions

2012


126.
F. Manjolinho, M. Arndt, K. Gooßen, L. J. Gooßen, ACS Catal. 2012, 2, 2014-2012: Catalytic C-H Carboxylation of Terminal Alkynes with Carbon Dioxide. >>DOI

125.
D. M. Ohlmann, N. Tschauder, J.-P. Stockis, K. Gooßen, M. Dierker, L. J. Gooßen, J. Am. Chem. Soc. 2012, 134, 13716-13729: Isomerizing Olefin Metathesis as a Strategy to Access Defined Distributions of Unsaturated Compounds from Fatty Acids. >>DOI

124.
F. Manjolinho, M. F. Grünberg, N. Rodríguez, L. J. Gooßen, Eur. J. Org. Chem. 2012, 4680-4683: Decarboxylative allylation of glyoxylic acids with diallyl carbonate. >>DOI

123.
P. Mamone, M. F. Grünberg, A. Fromm, B. A. Khan, L. J. Gooßen, Org. Lett. 2012, 14, 3716-3719: [Pd(μ-Br)(PtBu3)]2 as a Highly Active Isomerization Catalyst: Synthesis of Enol Esters from Allylic Esters. >>DOI

122.
S. Bhadra, W. I. Dzik, L. J. Gooßen, J. Am. Chem. Soc. 2012, 134, 9938-9941: Decarboxylative etherification of aromatic carboxylic acids. >>DOI

121.
A. Cotte, M. Gotta, L. J. Gooßen, F. Rudolphi, B. Song, WO2012066134, 2012, Preparing azomethine compounds comprises reacting alpha-oxocarboxylate compounds with aryl bromide compounds and amine compounds via alpha-iminocarboxylate intermediate compounds in presence of two transition metals as catalyst.

120.
W. I. Dzik, P. P. Lange, L. J. Gooßen, Chem. Sci. 2012, 3, 2671-2678: Carboxylates as Sources of Carbon Nucleophiles and Electrophiles: Comparison of Decarboxylative and Decarbonylative Pathways. >>DOI

119.
M. Arndt, E. Risto, T. Krause, L. J. Gooßen, ChemCatChem 2012, 4, 484-487: Silver(I) salts in combination with DMSO: unprecedented effective catalyst systems for the carboxylation of terminal alkynes at ambient CO2 pressure. >>DOI

118.
M. Hemgesberg, D. M. Ohlmann, Y. Schmitt, M. R. Wolfe, M. K. Müller, B. Erb, Y. Sun, L. J. Gooßen, M. Gerhards, W. R. Thiel, Eur. J. Org. Chem. 2012, 2142-2151: A Simple Access Sol-Gel Precursors Bearing Fluorescent Aromatic Core Units. >>DOI

117.
S. Tartaggia, O. De Lucchi, L. J. Gooßen, Eur. J. Org. Chem. 2012, 1431-1438: Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides. >>DOI

116.
T. Himmler, L. J. Gooßen, F. Rudolphi, B. Song, WO 2012116942, 2012 :Process for preparing aryl- and heteroarylacetic acid derivatives.

115.
M. Rudzki, A. Alcalde-Aragonés, W. I. Dzik, N. Rodríguez, L. J. Gooßen, Synthesis 2012, 44, 184-193: Selective Copper- or Silver-Catalyzed Decarboxylative Deuteration of Aromatic Carboxylic Acids. >>DOI

114.
B. A. Khan, A. E. Buba, L. J. Gooßen, Chem. Eur. J. 2012, 18, 1577-1581: Oxidative Trifluoromethylation of Arylboronates with Shelf-Stable Potassium (Trifluoromethyl)trimethoxyborate. >>DOI

113.
L. J. Gooßen, P. Mamone, C. Oppel, EP 2468708, 2012 :Preparing alkyl aryl ketones comprises heating blend comprising monocarboxylic acids e.g. benzene monocarboxylic acid, iron containing catalyst and solvent e.g. sulfolane, removing water and carbon dioxide from blend, and distilling blend.

112.
L. J. Gooßen, D. Ohlmann, M. Dierker, WO 2012055455, 2013 :Forming beta-functionalized carboxylic acid esters used as substrate for isomerization reaction involves reacting in one-pot, unsaturated ester in presence of boron compound/amine and rhodium containing catalyst under oxygen-free atmosphere.

111.
L. J. Gooßen, N. Rodríguez-Garrido, F. Manjolinho, P. Lange, WO 2012022801, 2013 :Preparing propiolic acid or its derivative comprises reacting a terminal alkyne with carbon dioxide in the presence of a base and a copper complex having at least one ligand.

110.
L. J. Gooßen, D. M. Ohlmann, M. Dierker, WO 2012143067, 2012 :Process for the production of unsaturated compounds.

2011


109.
F. Rudolphi, L. J. Gooßen, J. Chem. Inf. Model. 2011, 52, 293-301: Electronic Laboratory Notebook: The Academic Point of View. >>DOI

108.
N. Rodríguez, F. Manjolinho, M. F. Grünberg, L. J. Gooßen, Chem. Eur. J. 2011, 17, 13688-13691: Synthesis of a,b-Unsaturated Ketones via Pd-Catalyzed Decarboxylative Allylation of a-Oxocarboxylates. >>DOI

107.
F. Collet, B. Song, F. Rudolphi, L. J. Gooßen, Eur. J. Org. Chem., 2011, 6486-6501: Development of Decarboxylative Coupling Processes for the Synthesis of Azomethines and Ketones. >>DOI

106.
W. I. Dzik, L. J. Goossen, Angew. Chem., 2011, 123, 11241-11243: Selektive gekreuzte Tischtschenko-Reaktion – eine abfallfreie Synthese von Benzylestern. >>DOI; Angew. Chem. Int. Ed. 2011 , 50, 11047-11049: Selective Crossed Tishchenko Reaction – A Waste-Free Synthesis of Benzyl Esters. >>DOI

105.
B. Zimmermann, W. I. Dzik, T. Himmler, L. J. Goossen, J. Org. Chem., 2011, 76, 8107-8112: Palladium-catalyzed Cross-Coupling of Sterically Demanding Boronic Acids with a-Bromocarbonyl Compounds. >>DOI

104.
N. Rodríguez, L. J. Gooßen, Chem. Soc. Rev. 2011, 40, 5030-5048: Decarboxylative coupling reactions: a modern strategy for C–C-bond formation. >>DOI

103.
D. M. Ohlmann, L. J. Gooßen, M. Dierker, Chem. Eur. J. 2011, 17, 9508-9519: Regioselective synthesis of b-aryl- and b-amino-substituted aliphatic esters by rhodium-catalyzed tandem double-bond migration / conjugate addition. >>DOI

102.
B. Song, T. Himmler, L. J. Gooßen, Adv. Synth. Catal. 2011, 353, 1688-1694: Palladium/Copper-Catalyzed Di-alpha-arylation of Acetic Acid Esters. >>DOI

101.
M. Arndt, K. S. M. Salih, A. Fromm, L. J. Goossen, F. Menges, G. Niedner-Schatteburg, J. Am. Chem. Soc. 2011, 133, 7428-7449: Mechanistic Investigation of the Ru-Catalyzed Hydroamidation of Terminal Alkynes. >>DOI

100.
B. Song, F. Rudolphi, T. Himmler, L. J. Gooßen, Adv. Synth. Catal. 2011, 353, 1565-1574: Practical Synthesis of 2-Arylacetic Acid Esters via Palladium-Catalyzed Dealkoxycarbonylative Coupling of Malonates with Aryl Halides. >>DOI

99.
A. E. Buba, M. Arndt, L. J. Gooßen, J. Organomet. Chem. 2011, 696, 170-178: Z-Selective Hydroamidation of Terminal Alkynes with Secondary Amides and Imides Catalyzed by a Ru/Yb-System. >>DOI

98.
T. Knauber, F. Arikan, G.-V. Röschenthaler, L. J. Gooßen, Chem. Eur. J. 2011, 17, 2689-2697: Copper-Catalyzed Trifluoromethylation of Aryl Iodides with Potassium (Trifluoromethyl)trimethoxyborate. >>DOI

97.
P. P. Lange, L. J. Gooßen, P. Podmore, T. Underwood, N. Sciammetta, Chem. Commun. 2011, 47, 3628-3630: Decarboxylative biaryl synthesis in a continuous flow reactor. >>DOI

96.
L. J. Gooßen, F. Rudolphi, Chemie in unserer Zeit. 2011, 45, 56-57: Open Source Program: An Electronic Labjournal. >>DOI

95.
F. Rudolphi, B. Song, L. J. Gooßen, Adv. Synth. Catal. 2011, 353, 337-342: Synthesis of Azomethines from a-Oxocarboxylates, Amines and Aryl Bromides via One-Pot Three-Component Decarboxylative Coupling. >>DOI

94.
L. J. Gooßen, T. Knauber, EP 2366680, 2011: Process for the synthesis of 4`-haloalkyl-biphenyl-2-carboxylic acids.

93.
T. Himmler, L. J. Gooßen, B. Zimmermann, WO 2011089072, 2011: Process for the preparation of aryl- and heteroarylacetic acid derivatives.

92.
L. J. Gooßen, P. Mamone, C. Oppel, Adv. Synth. Catal. 2011, 353, 57-63: Catalytic Decarboxylative Cross-Ketonisation of Aryl- and Alkylcarboxylic Acids using Magnetite Nanoparticles. >>DOI

2010


91.
F. Rudolphi, L. J. Gooßen, Nachr. Chem. 2010, 5, 548-550: Ein elektronisches Laborjournal als Open-Source-Software. >>DOI

90.
F. Rudolphi, L. J. Gooßen, M. Stesycki, Chemie Report 2010, 5, 16-17: Leistungsstark und durchdacht - Fonds-Stipendiat entwickelt elektronisches Laborjournal.

89.
L. J. Gooßen, B. A. Khan, T. Fett, M. Treu, Adv. Synth. Catal. 2010, 352, 2166-2170: Low-pressure Hydrogenation of Arenecarboxylic Acids to Aryl Aldehydes. >>DOI

88.
L. J. Gooßen, F. Collet, K. Gooßen, Isr. J. Chem. 2010, 50, 617-629: Decarboxylative Coupling Reactions. >>DOI

87.
L. J. Gooßen, N. Rodríguez, K. Gooßen, McGraw-Hill Yearbook of Science and Technology 2010: Decarboxylative Couplings.

86.
L. J. Gooßen, N. Rodríguez, F. Manjolinho, P. P. Lange, Adv. Synth. Catal. 2010, 352, 2913-2917: Synthesis of Propiolic Acids via Cu-catalyzed Insertion of Carbon Dioxide into the C–H bond of Terminal Alkynes. >>DOI

85.
L. J. Gooßen, M. Blanchot, M. Arndt, K. S. M. Salih, Synlett 2010, 1685-1687: Synthesis of Botryllamides and Lansiumamides via Ru-Catalyzed Hydroamidation of Alkynes. >>DOI

84.
L. J. Gooßen, B. Zimmermann, T. Knauber, Beilstein J. Org. Chem. 2010, 6, No. 43.: Pd-catalyzed decarboxylative Heck vinylation of 2-nitrobenzoates in the presence of CuF2. >>DOI

83.
L. J. Gooßen, N. Rodríguez, C. Linder, P. P. Lange, A. Fromm, ChemCatChem 2010, 2, 430-442: Comparative Study of Copper- and Silver-Catalyzed Protodecarboxylations of Carboxylic Acids. >>DOI (Cover)

82.
L. J. Gooßen, P. P. Lange, N. Rodríguez, C. Linder, Chem. Eur. J. 2010, 16, 3906-3909: Low-Temperature Ag/Pd-Catalyzed Decarboxylative Cross-Coupling of Aryl Triflates with Aromatic Carboxylate Salts. >>DOI

81.
L. J. Gooßen, D. M. Ohlmann, M. Dierker, Green Chem. 2010, 12, 197-200: Silver Triflate-Catalysed Synthesis of γ-Lactones from Fatty Acids. >>DOI (Cover)

80.
L. J. Gooßen, N. Rodríguez, P. P. Lange, C. Linder, Angew. Chem. 2010, 122, 1129-1132: Decarboxylative Cross-Coupling of Aryl Tosylates with Aromatic Carboxylate Salts. >>DOI; Angew. Chem. Int. Ed. 2011 , 49, 1111-1114: Decarboxylative Cross-Coupling of Aryl Tosylates with Aromatic Carboxylate Salts. >>DOI

79.
L. J. Gooßen, D. M. Ohlmann, M. Dierker, T. Löhl, EP 10/2241562,2010: Process for the production of lactones.

2009


78.
L. J. Gooßen, N. Rodríguez, K. Gooßen, Angew. Chem. 2009, 121, 9770-9772: Stereoselektive Synthese von β-Chlorvinyl-substituierten Ketonen und Arenen durch katalytische Addition von Säurechloriden an Alkine. >>DOI; Angew. Chem. Int. Ed. 2009 , 48, 9592-9594: Stereoselective Synthesis of a-Chlorovinyl Ketones or Arenes by Catalytic Additions of Acid Chlorides to Alkynes. >>DOI

77.
L. J. Gooßen, C. Linder, N. Rodríguez, P. P. Lange, A. Fromm, Chem. Commun. 2009, 7173-7175: Silver-catalysed protodecarboxylation of carboxylic acids. >>DOI

76.
L. J. Gooßen, M. Blanchot, K. S. M. Salih, K. Gooßen, Synthesis 2009, 13, 2283-2288: Ruthenium-Catalyzed Addition of Primary Amides to Alkynes: A Stereoselective Synthesis of Secondary Enamides. >>DOI(highlighted in Synfacts 2009, 1, 85. >>DOI)

75.
L. J. Gooßen, C. Linder, N. Rodríguez, P. P. Lange, Chem. Eur. J. 2009, 15, 9336-9349 (Frontispiece): Biaryl and Aryl Ketone Synthesis via Pd-Catalyzed Decarboxylative Coupling of Carboxylate Salts with Aryl Triflates. >>DOI

74.
L. J. Gooßen, K. Gooßen. C. Stanciu, Angew. Chem. 2009, 121, 3621-3624: C(Aryl)-O-Aktivierung von Arylcarboxylaten in nickelkatalysierten Biarylsynthesen. >>DOI; Angew. Chem. Int. Ed. 2009 , 48, 3569-3571: Aryl-C–O-activation of Aryl Carboxylates in Nickel-Catalyzed Biaryl Syntheses (Highlight). >>DOI

73.
L. J. Gooßen, B. Zimmermann, C. Linder, N. Rodríguez, P. P. Lange, J. Hartung, Adv. Synth. Catal. 2009, 351, 2667-2674: Synthesis of Biaryls and Aryl Ketones via Microwave-Assisted Decarboxylative Cross-Couplings. >>DOI

72.
L. J. Gooßen, F. Manjolinho, B. A. Khan, N. Rodríguez, J. Org. Chem. 2009, 74, 2620-2623: Microwave assisted Cu-catalyzed protodecarboxylation of aromatic carboxylic acids. >>DOI

71.
L. J. Gooßen, D. M. Ohlmann, P. P. Lange, Synthesis 2009, 160-164: The Thermal Amidation of Carboxylic Acids Revisited. >>DOI

70.
A. Cotté, M. Gotta, L. J. Gooßen, F. Rudolphi, C. Oppel, N. Rodríguez, EP 09/2096101, 2009: Method for producing ketones from alpha-oxocarboxylates and aryl bromides.

2008


69.
L. J. Gooßen, M. Arndt, M. Blanchot, F. Rudolphi, F. Menges, G. Niedner-Schatteburg, Adv. Synth. Catal. 2008, 350, 2701-2707: A practical and effective RuCl3-based protocol for the regio- and stereoselective catalytic hydroamidation of terminal alkynes. >>DOI

68.
L. J. Gooßen, T. Knauber, J. Org. Chem. 2008, 73, 8631-8634: Concise Synthesis of Telmisartan via Decarboxylative Cross-Coupling. >>DOI

67.
L. J. Gooßen, N. Rodriguez, C. Linder, J. Am. Chem. Soc. 2008, 130, 15248-15249: Decarboxylative Biaryl Synthesis from Aromatic Carboxylates and Aryl Triflates. >>DOI

66.
L. J. Gooßen, M. Blanchot, K. S. M. Salih, R. Karch, A. Rivas-Nass, Org. Lett. 2008, 10, 4497-4499: Ruthenium-Catalyzed Stereoselective anti-Markovnikov-Addition of Thioamides to Alkynes. >>DOI

65.
L. J. Gooßen, K. S. M. Salih, M. Blanchot, Angew. Chem. 2008, 120, 8620-8623: Synthesis of Secondary Enamides via Ru-Catalyzed Selective Addition of Amides to Terminal Alkynes. >>DOI; Angew. Chem. Int. Ed. 2008 , 47, 8492-8495: Synthesis of Secondary Enamides via Ru-Catalyzed Selective Addition of Amides to Terminal Alkynes. >>DOI

64.
L. J. Gooßen, B. Zimmermann, T. Knauber, Angew. Chem. 2008, 120, 7211-7214: Pd/Cu-katalysierte decarboxylierende Kreuzkupplung von Arylchloriden und Kaliumcarboxylaten. >>DOI; Angew. Chem. Int. Ed. 2008 , 47, 7103-7106: Pd/Cu-catalyzed decarboxylative cross-coupling of aryl chlorides and potassium carboxylates. >>DOI

63.
L. J. Gooßen, N. Rodríguez, C. Linder, B. Zimmermann, T. Knauber, Org. Synth. 2008, 85, 196-204: Synthesis of 2-Substituted Biaryls via Cu/Pd-Catalyzed Decarboxylative Cross-Coupling of 2-Substituted Potassium Benzoates. >>DOI

62.
L. J. Gooßen, K. Gooßen, N. Rodríguez, M. Blanchot, C. Linder, B. Zimmermann, Pure Appl. Chem., 2008, 80, 1725-1731: New Catalytic Transformations of Carboxylic Acids. >>DOI

61.
L. J. Gooßen, K. Gooßen, Aktuelle Wochenschau der GDCh 2008, 18: Dream Reactions – Nachhaltigkeit durch atomökonomische Synthesen.

60.
L. J. Gooßen, N. Rodríguez, K. Gooßen, Angew. Chem. 2008, 120, 3144-3164: Katalytische Reaktionen von Carbonsäuren. >>DOI; Angew. Chem. Int. Ed. 2008 , 47, 3100 – 3120: Carboxylic acids as substrates in homogeneous catalysis. >>DOI

59.
L. J. Gooßen, F. Rudolphi, C. Oppel, N. Rodríguez, Angew. Chem. 2008, 120, 3085-3088: Synthese von Ketonen aus a-Ketocarboxylaten und Arylbromiden durch Cu/Pd-katalysierte decarboxylierende Kreuzkupplung. >>DOI; Angew. Chem. Int. Ed. 2008 , 47, 3043 –3045: Synthesis of Ketones from a-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling. >>DOI (Highlighted in Synfacts 2008, 6, 635. >>DOI

58.
A. Cotté, N. Mueller, L. Rodefeld, L. J. Gooßen, C. Linder, WO 08/122555, 2008: 2-Nitro-5-fluor-3’,4’-dichlorbiphenyl sowie ein Verfahren zu dessen Herstellung.

2007


57.
L. J. Gooßen, N. Rodríguez, Angew. Chem. 2007, 119, 7688-7690: Heterodimerisierung von Olefinen: Eine viel versprechende Strategie zur selektiven Synthese funktionalisierter Alkene. >>DOI; Angew. Chem. Int. Ed. 2007 , 46, 7544-7546: Heterodimerization of Olefins: A Highly Promising Strategy for the Selective Synthesis of Functionalized Alkenes. >>DOI

56.
L. J. Gooßen, B. Melzer, J. Org. Chem 2007, 72, 7473-7476: Synthesis of Valsartan via Decarboxylative Biaryl Coupling. >>DOI

55.
L. J. Gooßen, W. R. Thiel, N. Rodríguez, C. Linder, B. Melzer, Adv. Synth. Catal. 2007, 349, 2241-2246: Cu-catalyzed protodecarboxylation of aromatic carboxylic acids. >>DOI

54.
L. Gooßen, Angew. Chem. 2007, 119, 3865-3866: Metal-Catalysis in Industrial Organic Processes. Edited by Gian Paolo Chiusoli and Peter M. Maitlis (book review). >>DOI; Angew. Chem. Int. Ed. 2007 , 46, 3791-3792: Metal-Catalysis in Industrial Organic Processes. Edited by Gian Paolo Chiusoli and Peter M. Maitlis (book review). >>DOI

53.
L. J. Gooßen, N. Rodríguez, B. Melzer, C. Linder, G. Deng, L. M. Levy, J. Am. Chem. Soc. 2007, 129, 4824-4833: Biaryl Synthesis via Pd-Catalyzed Decarboxylative Coupling of Aromatic Carboxylates with Aryl Halides. >>DOI

2006 and earlier


52.
L. J. Gooßen, M. Blanchot, C. Brinkmann, K. Gooßen, R. Karch, A. Rivas-Nass, J. Org. Chem. 2006, 71, 9506-9509: Ru-Catalyzed Stereoselective Addition of Imides to Alkynes. >>DOI

51.
L. J. Gooßen, C. Linder, Synlett 2006, 3489-3491: Catalytic reductive etherification of ketones with alcohols at ambient hydrogen pressure: A practial, waste-minimized synthesis of dialkyl ethers. >>DOI

50.
L. J. Gooßen, G. Deng, L. M. Levy, Science 2006, 313 ,662-664: Synthesis of Biaryls via Catalytic Decarboxylative Coupling. >>DOI

49.
L. J. Gooßen, Koley, H. Hermann, W. Thiel, Organometallics 2006, 25 ,54-67: Palladium Monophosphine Intermediates in Catalytic Cross-Coupling Reactions: A DFT Study >>DOI

48.
L. J. Gooßen, K. Baumann, The Heck Reaction, in: Handbook of C-H Transformations: Applications in Organic Synthesis (G. Dyker, Ed.), Wiley-VCH, Weinheim, 2005. >>ISBN

47.
L. J. Gooßen, G. Deng, WO 06/136135, 2006: Verfahren zur decarboxylierenden C-C Verknüpfung von Carbonsäuren mit Kohlenstoffelektrophilen.

46.
L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, J. Am. Chem. Soc. 2005, 127 ,11102-11114: The Palladium-Catalyzed Cross-Coupling Reaction of Carboxylic Anhydrides with Arylboronic Acids: A DFT Study. >>DOI

45.
L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, Organometallics 2015, 24, 2398-2410: Mechanistic Pathways for Oxidative Addition of Aryl Halides to Palladium(0) Complexes:  A DFT Study. >>DOI

44.
L. J. Gooßen, J. E. Rauhaus, G. Deng, Angew. Chem. 2005, 117, 4110-4113: Ru-catalyzed anti-Markovnikov addition of amides to alkynes: A regio- and stereoselective synthesis of enamides. >>DOI; Angew. Chem. Int. Ed. 2005 44, 4042-4045: Ru-catalyzed anti-Markovnikov addition of amides to alkynes: A regio- and stereoselective synthesis of enamides. >>DOI

43.
L. J. Gooßen, M. K. Dezfuli, Synlett 2005, 445-448: Practical Protocol for the Palladium-Catalyzed Synthesis of Arylphosphonates from Bromoarenes and Diethyl Phosphite. >>DOI

42.
L. J. Gooßen, J. Paetzold, O. Briel, A. Rivas-Nass, Synlett 2005, 275-278: Buchwald-Hartwig Aminations of Aryl Chlorides: A Practical Protocol Based on Commercially Available Pd(0)-NHC Catalysts. >>DOI

41.
L. J. Gooßen, J. E. Rauhaus, WO 06/056166, 2006, 21, 17220-17223: Verfahren zur Addition von Amiden, Harnstoffen, Lactamen und Carbamaten an Alkine.

40.
L. J. Gooßen, J. Paetzold, Adv. Synth. Catal. 2004, 346, 1665-1668: New Synthesis of Biaryls via Rh-catalyzed Decarbonylative Suzuki-Coupling of Carboxylic Anhydrides with Arylboroxines. >>DOI

39.
L. J. Gooßen, Appl. Organomet. Chem. 2004, 18, 602-604: A Simple and Practical Protocol for the Pd-Catalyzed Cross-Coupling of Boronic Acids with Methyl Iodide. >>DOI

38.
L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, Chem. Commun. 2004, 2141-2143: The Mechanism of the Oxidative Addition of Aryl Halides to Pd-Catalysts: A DFT Investigation. >>DOI

37.
L. J. Gooßen, N. Rodriguez, Chem. Commun. 2004, 724-725: A Mild and Efficient Protocol for the Conversion of Carboxylic Acids to Olefins by a Catalytic Decarbonylative Elimination Reaction. >>DOI

36.
L. J. Gooßen, A. Döhring, Synlett 2004, 263-266: A Convenient Protocol for the Esterification of Carboxylic Acids with Alcohols in the Presence of Di-t-butyl Dicarbonate. >>DOI

35.
L. J. Gooßen, J. Paetzold, Angew. Chem. 2004, 116, 1115-1118: Decarbonylierende Heck-Olefinierung von Enolestern: salzfreier und umweltfreundlicher Zugang zu Vinylarenen. >>DOIAngew. Chem. Int. Ed. 2004, 43, 1095-1098: Decarbonylative Heck Olefination of Enol Esters: Salt-Free and Environmentally Friendly Access to Vinyl Arenes. >>DOI

34.
M. T. Reetz, L. J. Gooßen, A. Meiswinkel, J. Paetzold, J. Feldthusen Jensen, Org. Lett. 2003, 5, 3099-3101: Enantioselective Rh-Catalyzed Hydrogenation of Vinyl Carboxylates using Monodentate Phosphite Ligands. >>DOI

33.
L. J. Gooßen, A. Döhring, Adv. Synth. Catal. 2003, 345, 943-947: Lewis Acids as Highly Efficient Catalysts for the Decarboxylative Esterification of Carboxylic Acids with Dialkyl Dicarbonates. >>DOI

32.
L. J. Gooßen, J. Paetzold, D. Koley, Chem. Commun. 2003, 706-707: Regiocontrolled Ru-catalyzed Addition of Carboxylic Acids to Alkynes: Practical Protocols for the Synthesis of Vinyl Esters. >>DOI

31.
L. J. Gooßen, Angew. Chem. 2002, 114, 3929-3932: Asymmetrische Hydrovinylierung: neue perspektiven durch modulare Ligandensysteme (Highlight). >>DOIAngew. Chem. Int. Ed. 2002, 41, 3775-3778: Asymmetric Hydrovinylation: New Perspectives through Use of Modular Ligand Systems. >>DOI

30.
L. J. Gooßen, Angew. Chem. 2002, 114, 2971-2972:>>DOI ;Angew. Chem. Int. Ed. 2002, 41, 2845-2846: Cross-Coupling Reactions - A Practical Guide (book review). >>DOI

29.
. J. Gooßen, J. Paetzold, L. Winkel, Synlett 2002, 1721-1723: Pd-Catalyzed Decarbonylative Heck Olefination of Aromatic Carboxylic Acids activated in situ with Di-tert-butyl Dicarbonate. >>DOI

28.
L. J. Gooßen, L. Winkel, A. Döhring, K. Ghosh, J. Paetzold, Synlett 2002, 1237-1240: Pd-Catalyzed Synthesis of Functionalized Arylketones from Boronic Acids and Carboxylic Acids Activated in situ with Dimethyl Dicarbonate. >>DOI

27.
L. J. Gooßen, K. Ghosh, Eur. J. Org. Chem. 2002, 19, 3254-3256: Palladium-Catalyzed Synthesis of Arylketones from Boronic Acids and Carboxylic Acids Activated in situ by Pivalic Acid Anhydride. >>DOI

26.
L. J. Gooßen, K. Ghosh, Chem. Commun. 2002836-837: New Pd-Catalyzed Selective Reduction of Carboxylic Acids to Aldehydes. >>DOI

25.
L. J. Gooßen, J. Paetzold, WO 03/043958, 2003: Verfahren zur Herstellung von Vinylarenen und 1,3-Dienen aus Aryl- bzw. Vinylcarbonsäurederivaten.

24.
L. J. Gooßen, J. Paetzold, Angew. Chem. 2002, 114, 1285-1289: >>DOI;Angew. Chem. Int. Ed. 2002, 41, 1237-1241: Pd-Catalyzed Decarbonylative Olefination of Aryl Esters: Towards a Waste-Free Heck Reaction. >>DOI

23.
L. J. Gooßen, K. Baumann, Chemie in unserer Zeit 2001, 35, 402-403: Asymmetrische Katalyse.

22.
L. J. Gooßen, K. Ghosh, Chem. Commun. 2001, 20, 2084-2085: A New Practical Ketone Synthesis Directly from Carboxylic Acids: First Application of Coupling Reagents in Palladium Catalysis. >>DOI

21.
L. J. Gooßen, K. Ghosh (Studiengesellschaft Kohle m.b.H.), WO 02/092547, 2002,Verfahren zur Herstellung von Ketonen aus Carbonsäureanhydriden.

20.
L. J. Gooßen, K. Ghosh, Angew. Chem. 2001, 113, 3566-3568: >>DOI; Angew. Chem. Int. Ed. 2001, 40, 3458-3460: Palladium-Catalyzed Synthesis of Aryl Ketones from Boronic Acids and Carboxylic Acids or Anhydrides. >>DOI

19.
L. J. Gooßen (Studiengesellschaft Kohle m.b.H.), WO 02/072524, 2002: Verfahren zur Herstellung von Vinyl-, Aryl- und Heteroarylessigsäuren und ihrer Derivate.

18.
L. J. Gooßen, Chem. Commun. 2001, 7, 669-670: Palladium-Catalyzed Synthesis of Arylacetic Acid Derivatives from Boronic Acids. >>DOI

17.
L. J. Gooßen, A. S. Ferwanah, Synlett 2000, 2000, 1801-1803: A Mild and Efficient Protocol for the Catalytic Silylation of Aryl Bromides. >>DOI

16.
L. J. Gooßen, C. Heinemann, M. Jautelat, H. Greiving (Bayer AG), DE 10061202, 2002: Epoxidation and Hydrogenation Procedure for the Production of 1,6-Hexanediol from 1,5-Hexadiene.

15.
C. Heinemann, M. Jautelat, O. Kuhn, L. J. Gooßen, D. Ganzer (Bayer AG), DE 10064751, 2002: Verfahren zur Herstellung von Alk-3-en-1-olen.

14.
L. J. Gooßen, M. Jautelat, C. Heinemann, H. Greiving, K. Urtel, O. Kuhn (Bayer AG), patent WO 02/051780, 2002: Verfahren zur Herstellung von 1,6-Hexandiolen.

13.
L. J. Goossen, M. Hendrix (Bayer AG), EP 1157995, 2001: Preparation of Immobilized Palladium Complexes as Catalysts.

12.
L. J. Gooßen, H. Liu, K. R. Dress, K. B. Sharpless, Angew. Chem. 1999, 111, 1149-1152: Katalytische asymmetrische Aminohydroxylierung mit Amino-substituierten Heterocyclen als Stickstoffquelle. >>DOI; Angew. Chem. Int. Ed. 1999, 38, 1080-1083: Catalytic Asymmetric Aminohydroxylation with Amino-Substituted Heterocycles as Nitrogen Sources. >>DOI

11.
L. J. Gooßen, H. Liu, K. R. Dress, K. B. Sharpless, WO 00/10977, 2000: Catalytic Aminohydroxylation Using Amino-Substituted Heterocycles.

10.
K. R. Dress, L. J. Gooßen, H. Liu, D. Jerina, K. B. Sharpless, Tetrahedron Lett. 1998, 39, 7669-7672: Catalytic Aminohydroxylation with Adenine-Derivatives as Nitrogen Sources. >>DOI

9.
L. J. Gooßen, Funktionalisierte Imidazolin-2-yliden-Metallkomplexe in der Katalyse, Hieronymus Verlag, , München 1997, ISBN: 3-928286-88-9.

8.
W. A. Herrmann, L. J. Gooßen, M. Spiegler, Organometallics 1998, 17, 2162-2168: Chiral Imidazoline-2-ylidene-Oxazoline Metal Complexes. >>DOI

7.
W. A. Herrmann, L. J. Gooßen, M. Spiegler, J. Organomet. Chem. 1997, 547, 357-366: Functionalized Imidazoline-2-ylidene Complexes of Rhodium and Palladium. >>DOI

6.
W. A. Herrmann, L. J. Gooßen, G. R. J. Artus, C. Köcher, Organometallics 1997, 16, 2472-2477: Transition-Metal-Complexes of Chiral Imidazoline-2-ylidene Ligands. >>DOI

5.
W. A. Herrmann, L. J. Gooßen, C. Köcher, G. R. J. Artus, Angew. Chem. 1996, 108, 2980-2982: Chirale Heterocyclencarbene in der asymmetrischen Homogenkatalyse. >>DOI; Angew. Chem. It. Ed. 1996, 35, 2805-2807: Chiral Heterocylic Carbenes in Asymmetric Homogeneous Catalysis. >>DOI

4.
W. A. Herrmann, C. Köcher, L. J. Gooßen, G. R. J. Artus, WO 97/34875, 1997 Verfahren zur Herstellung heterocyclischer Carbene.

3.
W. A. Herrmann, C. Köcher, L. J. Gooßen, G. R. J. Artus, Chem. Eur. J. 1996, 2, 1627-1636: A High-Yielding Synthesis of Novel Functionalized N-Heterocyclic Carbenes in Liquid Ammonia. >>DOI

2.
M. D. Curtis, S. Druker, L. J. Gooßen, J. Kampf, Organometallics 1997, 16, 231-235: Structures of Anionic Mo/Co/S Cluster Salts. >>DOI

1.
J. Ashe III, L. J. Gooßen, J. Kampf, H. Konishi, Angew. Chem. 1992, 104, 1669-1670: Das erste Stibepin: Synthese und Struktur von Sb-Chlorbenzo[d]stibepin. >>DOI; Angew. Chem. Int. Ed. 1992, 31, 1642-1643: The First Stibepine: Synthesis and Structure of Sb-Chlorobenzo[d]stibepine. >>DOI