Asymmetric aldol reaction organocatalyzed by (S)-proline-containing dipeptides: Improved stereoinduction under solvent-free conditions

Journal of Organic Chemistry

Volumn 76, Issue 5, 2011, Pages 1464-1467

  Hernández, José G ^a   Juaristi, Eusebio ^a  

^a DEPARTAMENTO DE FÍSICA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC ALDEHYDE; ASYMMETRIC ALDOL REACTIONS; CYCLOHEXANONES; DI-PEPTIDES; DIASTEREO- AND ENANTIOSELECTIVITY; DIASTEREOMERIC RATIOS; DIPEPTIDE; ENANTIOMERIC EXCESS; METHYL ESTERS; ORGANOCATALYTIC; SOLVENT FREE CONDITIONS; STEREOSELECTIVE FORMATION;

ACETONE; ALDEHYDES; BALL MILLS; CONDENSATION REACTIONS; ENANTIOSELECTIVITY; ESTERS; PEPTIDES;

AMINO ACIDS;

PROLINE;

ALDOL REACTION; ARTICLE; CATALYSIS; ENANTIOMER; PROTEIN STRUCTURE;

ACETONE; ALDEHYDES; CATALYSIS; CYCLOHEXANONES; DIPEPTIDES; ESTERS; MOLECULAR STRUCTURE; PROLINE; STEREOISOMERISM;

EID: 79952124604     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1022469     Document Type: Article

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