A highly diastereoselective “super silyl” governed aldol reaction: synthesis of α,β-dioxyaldehydes and 1,2,3-triols-Reference-Cited by-同舟云学术

A highly diastereoselective “super silyl” governed aldol reaction: synthesis of α,β-dioxyaldehydes and 1,2,3-triols

Published:2016 Issue:1 Volume:7 Page:394-399
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Gati Wafa¹²³⁴^ORCID,Yamamoto Hisashi¹²³⁴^ORCID

Affiliation:

1. Molecular Catalyst Research Center

2. Chubu University

3. Kasugai

4. Japan

Abstract

“Super silyl” governed diastereoselective Mukaiyama aldol reaction for the construction of protected α,β-dioxyaldehydes and 1,2,3-triols via Lewis acid catalysis.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/SC/C5SC03307A

Reference38 articles.

1. D. A. Evans , J. V.Nelson and T.Taber, in Topics in Stereochemistry, Wiley, New York, 1982, vol. 13, p. 1

2. The Catalytic Asymmetric Aldol Reaction

3. The Aldol Addition Reaction: An Old Transformation at Constant Rebirth

4. NEW ALDOL TYPE REACTION

5. New Catalytic Concepts for the Asymmetric Aldol Reaction

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