Bifunctional chiral auxiliaries 3: Synthesis of homochiral 1,3-diols via asymmetric aldol reactions of dialkylboron enolates of 1,3-dipropionyl-trans-4,5-diphenyl-imidazolidin-2-one and aldehydes-Reference-Cited by-同舟云学术

Bifunctional chiral auxiliaries 3: Synthesis of homochiral 1,3-diols via asymmetric aldol reactions of dialkylboron enolates of 1,3-dipropionyl-trans-4,5-diphenyl-imidazolidin-2-one and aldehydes

Published:1991-01 Issue:10 Volume:2 Page:1001-1004
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Davies Stephen G.,Mortlock Andrew A.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference15 articles.

1. Practical enantioselective Diels-Alder and aldol reactions using a new chiral controller system

2. Enantioselective vicinal hydroxylation of terminal and E-1,2-disubstituted olefins by a chiral complex of osmium tetroxide. An effective controller system and a rational mechanistic model

3. A practical and efficient method for enantioselective allylation of aldehydes

4. A practical and general enantioselective synthesis of chiral propa-1,2-dienyl and propargyl carbinols

5. Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols

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