Enantioselective Michael additions to enones in their inclusion crystals with optically active host compounds
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference12 articles.
1. New synthetic methods. Secoalkylative approach to grandisol
2. ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE CYCLOHEXENOL DERIVATIVES VIA HIGHLY STEREOSELECTIVE REDUCTION OF (R)-3-(p-t-BUTYLPHENYLTHIO) CYCLOHEXAN-1-ONE
3. HIGHLY ENANTIOSELECTIVE MICHAEL ADDITION OF THIOLS TO 2-CYCLOHEXENONE BY USING (2S,4S)-2-(ANILINOMETHYL)-1-ETHYL-4-HYDROXYPYRRQLIPINE AS A CHIRAL CATALYST
4. ASYMMETRIC MICHAEL ADDITION OF THIOPHENOL TO MALEIC ACID ESTERS
5. Alkaloid catalyzed asymmetric synthesis III the addition of mercaptans to 2-cyclohexene-1-one; determination of enantiomeric excess using 13C NMR.
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4. ChemInform Abstract: Enantioselective Michael Additions to Enones in Their Inclusion Crystals with Optically Active Host Compounds.;ChemInform;2010-08-20
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