N-acylpyridinium trifluoromethanesulfonates and tetrafluoroborates: Shuttle reagents for the acylation of enantiopure secondary alcohols

Synthesis

Volumn , Issue 6, 1998, Pages 883-888

  Wagner, Rüdiger ^a   Günther, Wolfgang ^a   Anders, Ernst ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

Enantiopure secondary alcohols; Esterification; N acyl 4 benzylpyridinium trifluoromethanesulfonates or tetrafluoroborates; Shuttle reagents

Indexed keywords

FLUOROFORM; HETEROCYCLIC COMPOUND; N ACYL 4 BENZYLPYRIDINIUM TETRAFLUOBORATE; N ACYL 4 BENZYLPYRIDINIUM TRIFLUOROMETHANESULFONATE; N ACYLPYRIDINIUM TRIFLUOROMETHANESULFONATE; TETRAFLUOROBORATE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHIRALITY; ENANTIOMER; ESTERIFICATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RACEMIC MIXTURE; STEREOCHEMISTRY; SYNTHESIS;

EID: 0031744981     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-2074     Document Type: Article

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