Absolute Asymmetric Synthesis from Achiral Molecules in the Chiral Crystalline Environment
โ Scribed by Masami Sakamoto
- Book ID
- 102792901
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 506 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0947-6539
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โฆ Synopsis
Abstract
The current status of absolute asymmetric synthesis in a chiral crystalline environment has been reviewed. A number of topochemically controlled fourโcenter type photocycloadditions are described for a series of unsymmetrically substituted diolefin crystals and CT crystals. This concept has been applied to intramolecular photoreactions, and several successful absolute asymmetric syntheses have been achieved, involving Norrish Type II reaction, diโฯโmethane rearrangement, electrocyclization, thietane formation, oxetane formation, hydrogen abstraction by thiocarbonyl and alkenyl groups, and radicalโpair intermediates.
๐ SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
Solid State Photochemical Reaction of Achiral N-(ฮฒ,ฮณ-Unsaturated Carbonyl)thiocarbamate to Optically Active Thiolactone in the Chiral Crystalline Environment. -The solid-state photoreaction, leading to optically active ฮณ-thiolactone (II), proceeds via intramolecular [2 + 2] thietane formation and s