Stereodivergent Synthesis of Optically Activeα-Hydroxy Acids via Diastereoselective Reduction ofα-Keto Esters Derived from L-Quebrachitol
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/67/1/67_1_180/_pdf
Reference42 articles.
1. Remarkable optical induction in the reduction of .alpha.-oxo esters with B-(3-pinanyl)-9-borabicyclo[3.3.1]nonane. Synthesis of .alpha.-hydroxy esters of 100% optical purity
2. Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure .alpha.-hydroxy carboxylic acid synthons
3. Diastereoselective Reduction of α-Keto Amides Havingtrans-2,5-Disubstituted Pyrrolidine as a Chiral Auxiliary
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