Erythroselective aldol condensation of amine Free 2-t-butyl-5-methyl-2-phenyl-1,3-dioxolan-4-one lithium enolate synthesis of the ethyl acetolactate enantiomers-Reference-Cited by-同舟云学术

Erythroselective aldol condensation of amine Free 2-t-butyl-5-methyl-2-phenyl-1,3-dioxolan-4-one lithium enolate synthesis of the ethyl acetolactate enantiomers

Published:1992-03 Issue:14 Volume:33 Page:1897-1900
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Greiner Alfred,Ortholand Jean-Yves

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Optically active 2-ethenyl-1,3-dioxolanones as 3-carbon synthons. Allylnickel derivatives as homoenolate equivalents

2. Chirality transfer from lactic acid selective synthesis of 2,2-disubstituted-1,3-dioxolan-4-ones from ketones and acetals

3. Biosynthesis of valine and isoleucine: synthesis and biological activity of (2S)-α-acetolactic acid (2-hydroxy-2-methyl-3-oxobutanoic acid), and (2R)- and (2S)-α-acetohydroxybutyric acid (2-ethyl-2-hydroxy-3-oxobutanoic acid)

4. Stereochemistry of valine and isoleucine biosynthesis

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