An inexpensive and selective oxygenation of N-alkyl imines to oxaziridines

Synlett

Volumn , Issue 7, 2005, Pages 1176-1178

  Shailaja, M ^a   Manjula, A ^a   Rao, B Vittal ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Imines; Oxaziridine; Oxidation; Peroxide; Sodium tungstate

Indexed keywords

ACETONITRILE; ALKYL GROUP; BENZONITRILE; HYDROGEN PEROXIDE; IMINE; OXAZIRIDINE DERIVATIVE; PEROXIDE; SODIUM TUNGSTEN; SOLVENT; TUNGSTEN DERIVATIVE; UNCLASSIFIED DRUG;

CHEMICAL BOND; CHEMICAL REACTION; CONCENTRATION RESPONSE; CONFERENCE PAPER; DIASTEREOISOMER; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRON TRANSPORT; ISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; OXYGENATION; REACTION ANALYSIS; REPRODUCIBILITY; STEREOCHEMISTRY;

EID: 18744406768     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-865219     Document Type: Conference Paper

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29. 4(anhyd) and evaporated. The crude product was purified by column chromatography on silica gel using mixtures of hexane and EtOAc.