Nguồn ngoài

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.

Organic Chemistry Chemistry

Tác giả: R. Balaji Rao
Nhà xuất bản: Banaras Hindu University
Nguồn: LibreTexts
Giấy phép: CC BY-NC-ND
Ngôn ngữ: EN
Danh mục: Khoa học cơ bản

Đọc trực tuyến Tải PDF (nguồn mở)

Mục lục· 19 mục

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