Highly Enantioselective Synthesis of Propargylic Alcohols by Way of the Asymmetric Aldol Reaction
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/20/6/20_6_989/_pdf
Reference16 articles.
1. Reduction of .alpha.,.beta.-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane. High asymmetric induction in aliphatic systems
2. Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agent
3. Reductive cleavages of α, β-alkynyl acetals. New route to optically pure propargylic alcohols
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