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Logic of Organic Synthesis
A mastery over several such techniques enables the molecular architect (popularly known as organic chemist) to achieve the challenging task of synthesizing the myriade of molecular structures encountered in Natural Products Chemistry, Drug Chemistry and modern Molecular Materials. In this task, organic chemists are further guided by several ‘thumb rules’ that chemists have evolved over the past two centuries.
- Author
- R. Balaji Rao
- Publisher
- Banaras Hindu University
- Source
- LibreTexts
- License
- CC BY-NC-ND
- Language
- EN
- Category
- Basic Sciences
Contents· 19 sections
- 01: Synthesis of Organic Molecules
- 02: Rules and Guidelines Governing Organic Synthesis
- 2.01: Baldwins Rule for Ring Closure Reactions
- 2.02: Bredt's Rule
- 2.03: Cram's Rule and Prelog's Rule
- 2.04: Hofmanns Rule and Zaitsevs Rule
- 2.05: Markovnikov Rule
- 03: Criteria for Selection of the Synthetic Route
- 04: The Logic of Synthesis
- 05: Strategies in Disparlure Synthesis
- 06: Strategies in (-)-Menthol Synthesis
- 07: Strategies in Longifolene Synthesis
- 08: Strategies in Cedrene Synthesis
- 09: Strategies in Reserpine Synthesis
- 10: Strategies in Prostaglandins Synthesis
- 11: Strategies in Steroids Synthesis
- 12: Woodwards Synthesis of Chlorophyll
- 13: Synthesis of Vitamin B
- 14: Green Chemistry - Protection-Free Organic Synthesis