SmI2-Induced highly regioselective reduction of α,β-epoxy esters and γ,δ-epoxy-α,β-unsaturated esters. An efficient route to optically active β-hydroxy and δ-hydroxy esters-Reference-Cited by-同舟云学术

SmI2-Induced highly regioselective reduction of α,β-epoxy esters and γ,δ-epoxy-α,β-unsaturated esters. An efficient route to optically active β-hydroxy and δ-hydroxy esters

Published:1987-01 Issue:38 Volume:28 Page:4437-4440
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Otsubo Kenji,Inanaga Junji,Yamaguchi Masaru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. SmI2-induced reductive cross-coupling of carbonyl compounds with (α,β-unsaturated esters

2. K. Otsubo, K. Kawamura, J. Inanaga, and M. Yamaguchi, Chem. Lett., in press.

3. K. Otsubo, J. Inanaga, and M. Yamaguchi, the preceding paper.

4. Organometallic Derivatives of Epoxides

5. Lanthanides in organic synthesis. 4. Reduction of .alpha.,.beta.-epoxy ketones with samarium diiodide. A route to chiral, nonracemic aldols

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