Electrophilic 5-endo-trig Cyclizations of 2-Silyl-3-alkenols. A Stereoselective Route to Polysubstituted Tetrahydrofurans. -The scope and limitations of the 5-endo-trig-like cyclization of 9 2-silyl-3-alkenols, e.g. (I), to give tetrahydrofurans, e.g. (III), is investigated. The regioselectivity see
ChemInform Abstract: Stereoselective Synthesis of Substituted Tetrahydrofurans Using 5-Endo-trig Cyclization Reactions.
β Scribed by Donald Craig; Neil J. Ikin; Neil Mathews; Alison M. Smith
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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β¦ 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 βFull Textβ option. The original article is trackable v
## 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 βFull Textβ option. The original article is trackable v