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Asymmetric cleavage of chiral α,β-ethylenic acetals by organolithium reagents

✍ Scribed by Alexandre Alexakis; Farida Mhamdi; Franz Lagasse; Pierre Mangeney

Book ID
118606573
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
187 KB
Volume
7
Category
Article
ISSN
0957-4166

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📜 SIMILAR VOLUMES

ChemInform Abstract: Asymmetric Cleavage
ChemInform Abstract: Asymmetric Cleavage of Chiral α,β-Ethylenic Acetals by Organolithium Reagents.
✍ A. ALEXAKIS; F. MHAMDI; F. LAGASSE; P. MANGENEY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

## 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

Asymmetric reduction of ketone reductive
Asymmetric reduction of ketone reductive cleavage of chiral acetals using organoaluminum reagents
✍ Atsunori Mori; Junya Fujiwara; Keiji Maruoka; Hisashi Yamamoto 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 229 KB

Some chiral acetals are cleaved by organoaluminum reagents. The products are formed diastereoselectively, and the removal of the chiral auxiliary affords optically active alcohols. A recent communication by Bartlett, Johnson and Elliott1 on the acetal derived from (-)-(2$4\_R)-2,4-pentanediol has pr