An efficient strategy for the synthesis of syn 1,3-diols via iterative acetate aldol reactions and synthesis of atorvastatin lactone-Reference-Cited by-同舟云学术

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An efficient strategy for the synthesis of syn 1,3-diols via iterative acetate aldol reactions and synthesis of atorvastatin lactone

Published:2015-09 Issue:40 Volume:56 Page:5409-5412
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Goyal Sandeep,Patel Bhautikkumar,Sharma Ratnesh,Chouhan Mangilal,Kumar Kapil,Gangar Mukesh,Nair Vipin A.

Funder

Department of Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference66 articles.

1. STEREOSELECTIVE SYNTHESIS OFMESO(ORERYTHRO) 1,3-DIOLS FROM β-HYDROXYKETONES

2. Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelates

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

4. A Novel Method for the In situ Generation of Alkoxydialkylboranes and Their Use in the Selective Preparation of 1,3-synDiols

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