A new synthetic route to 3-Oxo-4-amino-1, 2, 3-oxadiazole from the diazeniumdiolation of benzyl cyanide: Stable sydnone iminium N-Oxides

Journal of Organic Chemistry

Volumn 74, Issue 4, 2009, Pages 1621-1626

  Scott Bohle, D ^a   Perepichka, Inna ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO TAUTOMERS; BENZYL CYANIDES; IMINIUM; OXADIAZOLE; OXADIAZOLES; SALICYLALDEHYDE; SCHIFF-BASE; SEPARATION AND PURIFICATIONS; SYNTHETIC ROUTES; THEORETICAL CALCULATIONS;

AMINATION; CYANIDES; METHANOL; NITRIC OXIDE;

AMINES;

3 OXO 4 AMINO 1,2,3 OXADIAZOLE; 3 OXO 4 PHENYL 5 AMINO 1,2,3 OXADIAZOLE; BENZYL CYANIDE DERIVATIVE; IMINE; NITRIC OXIDE; OXADIAZOLE DERIVATIVE; OXIDE; SCHIFF BASE; SYDNONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DENSITY FUNCTIONAL THEORY; GEOMETRY; HYDROGEN BOND; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION;

EID: 64349117188     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802343k     Document Type: Article

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