On the steric course of the addition of some organometallic reagents to (R)-2,3-isopropylidene glyceraldehyde. Synthesis of optically active α-benzyloxy aldehydes, alcohols, carboxylic acids and 1,2-diols.-Reference-Cited by-同舟云学术

On the steric course of the addition of some organometallic reagents to (R)-2,3-isopropylidene glyceraldehyde. Synthesis of optically active α-benzyloxy aldehydes, alcohols, carboxylic acids and 1,2-diols.

Published:1983-01 Issue:28 Volume:24 Page:2843-2846
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mulzer Johann,Angermann Alfred

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. On the steric course of the addition of diallylzinc onto α,β-dialkoxy chiral carbonyl compounds: stereospecific synthesis of 2,6-dideoxysugars of the -series

2. AN ASYMMETRIC SYNTHESIS OF α-BENZYLOXY ALDEHYDES HAVING A CHIRAL TERTIARY CENTER—AN APPLICATION TO THE ASYMMETRIC SYNTHESIS OFexo-(+)-BREVICOMIN—

3. Enantiomerenreine Synthesevorstufen ausD-Galactodialdehyd

4. Use of a Grignard reagent to lengthen a triose carbon chain

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