Issue 6, 1985

Acyclic stereoselection using relative 1,2-asymmetric induction. A convenient method for the stereoselective construction of α,γ-dimethyl-α,β-dihydroxy compounds, useful intermediates for synthesis of erythronolides

Abstract

Highly Stereoselective addition of dithiane anions with 2-methyl-3-trimethylsilylbut-3-enal combined with the stereoselective addition of Grignard reagents to chiral α-alkoxyketones affords a practical and efficient method for the construction of the title compounds.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 329-330

Acyclic stereoselection using relative 1,2-asymmetric induction. A convenient method for the stereoselective construction of α,γ-dimethyl-α,β-dihydroxy compounds, useful intermediates for synthesis of erythronolides

A. K. Samaddar, T. Chiba, Y. Kobayashi and F. Sato, J. Chem. Soc., Chem. Commun., 1985, 329 DOI: 10.1039/C39850000329

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