Regio- and stereocontrolled syntheses of cyclic chiral cis-amino alcohols from 1,2-diols or epoxides-Reference-Cited by-同舟云学术

Regio- and stereocontrolled syntheses of cyclic chiral cis-amino alcohols from 1,2-diols or epoxides

Published:1995-10 Issue:42 Volume:36 Page:7615-7618
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Senanayake Chris H.,DiMichele Lisa M.,Liu Ji,Fredenburgh Laura E.,Ryan Kenneth M.,Edward Roberts F.,Larsen Robert D.,Verhoeven Thomas R.,Reider Paul J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

1. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification

2. The chiral pool as a source of enantioselective catalysts and auxiliaries

3. Enantioselective addition of organozinc reagents to aldehydes

4. Highly diastereoselective reaction of a chiral, non-racemic amide enolate with (S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524

5. Chemo-enzymatic synthesis of 1,2- and 1,3- amino-alcohols and their use in the enantioselective reduction of acetophenone and anti-acetophenone oxime methyl ether with borane.

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