A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction

Journal of Organic Chemistry

Volumn 75, Issue 21, 2010, Pages 7099-7106

  Gassa, Federico ^a   Contini, Alessandro ^a   Fontana, Gabriele ^b   Pellegrino, Sara ^a   Gelmi, Maria Luisa ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b INDENA S P A   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVES; AMINO ESTERS; BENZYLAMINES; COMPUTATIONAL MODEL; DIASTEREOSELECTION; DIASTEREOSELECTIVE SYNTHESIS; KETENE SILYL ACETAL; KEY REACTIONS; LEWIS ACID; SYNTHETIC PROTOCOLS; THREE-COMPONENT;

ALDEHYDES; AMINO ACIDS; ESTERS; SYNTHESIS (CHEMICAL);

CONDENSATION REACTIONS;

ACETAL DERIVATIVE; ALDEHYDE; AMINO ACID DERIVATIVE; BENZYLAMINE; ESTER DERIVATIVE; LACTONE DERIVATIVE; LEWIS ACID;

ARTICLE; CATALYSIS; CHEMICAL REACTION; METHANOLYSIS; STEREOCHEMISTRY; SYNTHESIS;

ALDEHYDES; AMINES; AMINO ACIDS; CATALYSIS; ETHYLENES; KETONES; LEWIS ACIDS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 78049514685     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1011762     Document Type: Article

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