An efficient method for the stereoselective synthesis of cis-3-substituted prolines: Conformationally constrained α-amino acids

Tetrahedron

Volumn 58, Issue 52, 2002, Pages 10475-10484

  Flamant Robin, Céline ^a   Wang, Qian ^a   Chiaroni, Angèle ^a   Sasaki, N André ^a  

^a CNRS   (France)

Author keywords

3 cis substituted proline; Conformationally constrained amino acid; Organocuprate; Stereoselective

Indexed keywords

3 VINYLPYRROLIDINE 1,2 DICARBOXYLIC ACID 1 TERT BUTYL ESTER 2 METHYL ESTER; 4 (2' ETHOXYCARBONYLVINYL) 2,2 DIMETHYLOXAZOLIDINE 3 CARBOXYLIC ACID TERT BUTYL ESTER; ALDEHYDE; AMINO ACID DERIVATIVE; ESTER DERIVATIVE; PROLINE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CONFORMATION; CRYSTAL STRUCTURE; CYCLIZATION; ENANTIOMER; MASS SPECTROMETRY; OXIDATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS; X RAY ANALYSIS;

EID: 0037164661     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01405-9     Document Type: Article

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