Two-step stereoselective conversion of 5-monosubstituted 1,3-dioxolan-4-ones into selectively protected 2,3-erythro-1,2,3-triols. A route to polyhydroxylated molecules-Reference-Cited by-同舟云学术

Two-step stereoselective conversion of 5-monosubstituted 1,3-dioxolan-4-ones into selectively protected 2,3-erythro-1,2,3-triols. A route to polyhydroxylated molecules

Published:1994-04 Issue:16 Volume:35 Page:2537-2540
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Untersteller Edouard,Chao Xin Yan,Sinaÿ Pierre

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. (α-Alkylation of α-heterosubstituted carboxylic acids without racemization

2. Preparation of 5-alkyl-2-tert-butyl-1,3-dioxolan-4-ones by trimethylsilyl triflate catalyzed reactions between bis(trimethylsilyl) derivatives of .alpha.-hydroxycarboxylic acids and pivaldehyde

3. Spiro asymmetric induction. Synthesis of optically pure .alpha.-hydroxy acid derivatives by alkylation of a chiral glycolate enolate

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