New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet-Hauser rearrangements

Organic and Biomolecular Chemistry

Volumn 6, Issue 20, 2008, Pages 3673-3680

  Tayama, Eiji ^a   Orihara, Kiwako ^a   Kimura, Hiroshi ^a  

^a NIIGATA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINATION; AMINES; AMMONIUM COMPOUNDS; ORGANIC ACIDS; SALTS;

AMINO ACID DERIVATIVES; AMMONIUM SALTS; BENZYLIC; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE; OPTICALLY ACTIVE; SYNTHETIC ROUTES;

AMINO ACIDS;

AMINO ACID; BUTANOL; TERT BUTOXIDE, POTASSIUM; TERT-BUTOXIDE, POTASSIUM;

ARTICLE; CHEMISTRY; ENZYME SPECIFICITY; OPTICS; STEREOISOMERISM; SYNTHESIS;

AMINO ACIDS; BUTANOLS; OPTICS AND PHOTONICS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 53549085393     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b811162f     Document Type: Article

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