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Carbonyl addition reaction by means of β-silyl- and βstannylphosphorous ylides: Diastereoselective E-propenylation of α-chiral aldehydes

✍ Scribed by Masamitsu Tsukamoto; Hideo Iio; Takashi Tokoroyama


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
286 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


E-Propenylation

of aldehydes using a-silyl-or 8-stannylphosphorous ylides is devised, and extended to the diastereoselective reaction of a-methyl and a-alkoxy aldehydes.

We have recently reported that the 8-silylphosphorous ylides la and lb provide vinyl and isopropenyl alcohols with high 1,2-asymmetric induction, respectively, in the reaction of a-chiral aldehydes. r In this paper we describe


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ChemInform Abstract: Diastereoselective
✍ Jose M. Andres; Rafael Pedrosa; Alberto Perez; Alfonso Perez-Encabo 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

## 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