The trisubstituted functionalized tetrahydrofurans 10, 11, 16, 18, and 19 were photochemically prepared from 2,3-syn-and 2,3-anti-configured N-(3-benzoyloxy-5-hexen-2-oxy)thiazole-2(3H)-thione anti-6, pyridinethiones 7, anti-8, and BrCCl 3 . The formation of tetrahydrofurans was achieved by an effic
ChemInform Abstract: Ring Closure Reactions of Disubstituted 4-Penten-1-oxyl Radicals — Towards a Stereoselective Synthesis of allo-Muscarine.
✍ Scribed by Jens Hartung; Rainer Kneuer
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 34 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v