Diastereoselective reduction of α-keto esters bearing chiro-inositol derivatives as chiral auxiliaries
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 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. ASYMMETRIC REDUCTION OF PROCHIRAL KETO ESTERS WITH A CHIRAL REDUCING AGENT PREPARED FROM TIN(II) CHLORIDE, CHIRAL DIAMINE, AND DIISOBUTYLALUMINUM HYDRIDE
4. ASYMMETRIC HYDROGENATION OFN-(α-KETOACYL)-α-AMINO ESTERS
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