Application of erythro-2-amino-1,2-diphenylethanol as a highly efficient chiral auxiliary. Highly stereoselective Staudinger-type β-lactam synthesis using a 2-chloro-1-methylpyridinium salt as the dehydrating agent

Synthesis

Volumn , Issue 8, 1998, Pages 1161-1166

  Matsui, Satoshi ^a   Hashimoto, Yukihiko ^a   Saigo, Kazuhiko ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

(1S,2R) 2 amino 1,2 diphenylethanol; 2 chloro 1 methylpyridinium salt; Staudinger type reaction; 2+2 cycloaddition; lactams

Indexed keywords

2 CHLORO 1 METHYLPYRIDINIUM; BETA LACTAM; ERYTHRO 2 AMINO 1,2 DIPHENYLETHANOL; PYRIDINIUM DERIVATIVE; UNCLASSIFIED DRUG;

CHIRALITY; CONTROLLED STUDY; DEHYDRATION; DRUG SYNTHESIS; ENANTIOMER; NONHUMAN; SHORT SURVEY; STEREOCHEMISTRY;

EID: 0031871452     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-2117     Document Type: Short Survey

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