Highly Enantioselective Synthesis of Tertiary Boronic Esters and their Stereospecific Conversion to other Functional Groups and Quaternary Stereocentres-Reference-Cited by-同舟云学术

Highly Enantioselective Synthesis of Tertiary Boronic Esters and their Stereospecific Conversion to other Functional Groups and Quaternary Stereocentres

Published:2011-11-03 Issue:47 Volume:17 Page:13124-13132
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Scott Helen K.,Aggarwal Varinder K.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201102581/fullpdf

Reference99 articles.

1. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems

2. Hydroboration of Terpenes. II. The Hydroboration of α- and β-Pinene-The Absolute Configuration of the Dialkylborane from the Hydroboration of α-Pinene

3. Hydroboration. XVIII. The Reaction of Diisopinocampheylborane with Representative cis-Acyclic, Cyclic, and Bicyclic Olefins. A Convenient Systhesis of Optically Active Alcohols and Olefins of High Optical Purity and Established Configuration

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