Asymmetric synthesis of 3,5-dihydroxy-6(E)-heptenoate-containing HMG-CoA reductase inhibitors-Reference-Cited by-同舟云学术

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Asymmetric synthesis of 3,5-dihydroxy-6(E)-heptenoate-containing HMG-CoA reductase inhibitors

Published:1997-08 Issue:31 Volume:53 Page:10659-10670
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tempkin Orin,Abel Stephan,Chen Chung-Pin,Underwood Russell,Prasad Kapa,Chen Kau-Ming,Repic Oljan,Blacklock Thomas J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. HMG‐CoA Reductase Inhibitors: An Exciting Development in the Treatment of Hyperlipoproteinemia

2. A highly stereoselective route to the four stereoisomers of a six-carbon synthon

3. A General Method for the Synthesis ofsyn-(E)-3,5-Dihydroxy-6-heptenoates

4. 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranes

5. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

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