Organische chemie II - AG Organische Synthese und Katalyse

Prof. Gerald Dyker - VideoVorlesungen

Videokanal der RUB: www.youtube.com/user/ChemieRUB

Organic Synthesis III: Designing organic syntheses

Winter semester 2014/15

• Lecture Designing Organic Syntheses 1
  - Key terms of retrosynthetic analysis: synthon, retron, synthetic equivalent 07.10.2014

• Lecture Designing Organic Syntheses 2
  - Retron of oxy-Cope rearrangement 08.10.2014

• Lecture Designing Organic Syntheses 3
  - Key terms of retrosynthetic analysis: synthon, retron, synthetic equivalent 14.10.2014

• Lecture Designing Organic Syntheses 4
  - Additional Strategies and Tactics in Retrosynthetic Analysis 15.10.2014

• Lecture Designing Organic Syntheses 5
  - Carbon-heteroatom bonds as strategic bonds 24.10.2014

• Lecture Designing Organic Syntheses 6
  - Difunctional Compounds 28.10.2014

• Lecture Designing Organic Syntheses 7
  - 1,2-, 1,3- and 1,4-Dicarbonyl Compounds 29.10.2014

• Lecture Designing Organic Syntheses 8
  - 1,5- and 1,6-Dicarbonyl Compounds 31.10.2014

• Lecture Designing Organic Syntheses 9
  - Carbonyl Combinations in Retrosynthetic Analysis 04.11.2014

• Lecture Designing Organic Syntheses 10
  - Stereocontrol in Retrosynthetic Analysis 05.11.2014

• Lecture Designing Organic Syntheses 11
  - Target Molecules with Adjacent Stereocenters 11.11.2014

• Lecture Designing Organic Syntheses 12
  - Aliphatic Heterocycles 12.11.2014

• Lecture Designing Organic Syntheses 13
  - Hetarenes: Furans, Pyrrols and Thiophenes 19.11.2014

• Lecture Designing Organic Syntheses 14
  - Hetarenes: Indoles, Benzofurans, Pyridines, Quinolines, Isoquinolines 25.11.2014

• Lecture Designing Organic Syntheses 15
  - Hetarenes: Oxazoles, Isoxazoles, Thiazoles, Imidazoles, Pyrazoles, Triazoles 26.11.2014

• Lecture Designing Organic Syntheses 16
  - Conjunctive Reagents 02.12.2014

• Lecture Designing Organic Syntheses 17
  - Epibatidine: Retrosynthetic Analysis 03.12.2014

• Lecture Designing Organic Syntheses 18
  - Epibatidine: Enantioselective Synthesis 09.12.2014

• Lecture Designing Organic Syntheses 19
  - Epothilone: Retrosynthetic Analysis 10.12.2014

• Lecture Designing Organic Syntheses 20
  - Special Hydrocarbons: “Fixed” Conformers of Cyclohexane 17.12.2014

• Lecture Designing Organic Syntheses 21
  - Carbon Frameworks Resembling Polyhedrons 07.01.2015

• Lecture Designing Organic Syntheses 22
  - Terpenoid Hydrocarbons 13.01.2015

• Lecture Designing Organic Syntheses 23
  - Free Radical Cyclizations 16.01.2015

• Lecture Designing Organic Syntheses 24
  - Mannich Reactions in Alkaloid Syntheses 21.01.2015

• Lecture Designing Organic Syntheses 25
  - Magic Mannich 1: Aza-Cope Mannich Combinations 22.01.2015

• Lecture Designing Organic Syntheses 26
  - Magic Mannich 2: Domino Processes with Iminium Cations 28.01.2015

• Lecture Designing Organic Syntheses 27
  - Targeting Red Tide Toxins: Brevetoxin B 04.02.2015

• Lecture Designing Organic Syntheses 28
  - The Universal Retron of the Ring Closing Olefin Metathesis 06.02.2015

• Lecture Designing Organic Syntheses 29
  - Lasso Mechanisms and Voodoo Chemistry: Two Common Misconceptions 19.07.2016