𝔖 Scriptorium
✦   LIBER   ✦

πŸ“

Cycloaddition Reactions in Organic Synthesis

✍ Scribed by Shū Kobayashi, Karl Anker Jorgensen


Publisher
Wiley-VCH
Year
2001
Tongue
English
Leaves
344
Edition
1
Category
Library

⬇  Acquire This Volume

No coin nor oath required. For personal study only.

✦ Synopsis


Cycloaddition reactions are among the most important tools for synthesis in organic chemistry, since these reactions are vital to the modern synthesis of natural products and biologically active substances. Metal catalysis plays an increasingly important role in these reactions, often allowing several stereocenters to be selectively created and integrated in the target molecules. Kobayashi and Jorgensen's handbook provides numerous examples of metal-catalyzed reactions, including [2+1], [3+2] and [4+2] cycloadditions. Important reactions such as carbo- and hetero-Diels-Alder, carbocyclic, cyclopropanation and 1,3-dipolar cycloaddition reactions are discussed. A large number of experimental procedures gives a concrete idea of the use of metal-catalyzed cycloaddition reactions in modern synthesis. The book is aimed at chemists in industry or academia, who want to effectively use cycloadditions in their work.


πŸ“œ SIMILAR VOLUMES


Cycloaddition Reactions in Organic Synth
✍ Shū Kobayashi, Karl Anker Jorgensen πŸ“‚ Library πŸ“… 2001 πŸ› Wiley-VCH 🌐 English

Cycloaddition reactions are among the most important tools for synthesis in organic chemistry, since these reactions are vital to the modern synthesis of natural products and biologically active substances. Metal catalysis plays an increasingly important role in these reactions, often allow

Cycloaddition Reactions in Organic Synth
✍ Karola RΓΌck-Braun πŸ“‚ Library πŸ“… 1999 πŸ› Wiley-VCH 🌐 English

Since the days of Diels, Alder and Woodward, cycloadditions have been among the most versatile reactions for stereoselective synthesis ... All relevant information is collected in this well-structured, practical handbook. Arranged according to the cycloaddition type, the suitable auxiliari