Synthesis of methyl-1-(tert -butoxycarbonylamino)-2- vinylcyclopropanecarboxylate via a hofmann rearrangement utilizing trichloroisocyanuric acid as an oxidant

Journal of Organic Chemistry

Volumn 76, Issue 1, 2011, Pages 277-280

  Crane, Zackary D ^a   Nichols, Paul J ^a   Sammakia, Tarek ^a   Stengel, Peter J ^a  

^a Array Bio Pharma Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPYL; HOFMANN REARRANGEMENT; NITRO GROUP; PYRIDYL; TRICHLOROISOCYANURIC ACID;

FUNCTIONAL GROUPS;

SYNTHESIS (CHEMICAL);

BENZENE; CARBOXYLIC ACID DERIVATIVE; CYANURIC ACID; CYCLOPROPANE DERIVATIVE; FUNCTIONAL GROUP; METHYL 1 (TERT BUTOXYCARBONYLAMINO) 2 VINYLCYCLOPROPANECARBOXYLATE; NITRO DERIVATIVE; OXIDIZING AGENT; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRIDINE; SYMCLOSENE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; HOFMANN REARRANGEMENT; OXIDATION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

MAGNETIC RESONANCE SPECTROSCOPY; OXIDANTS; STEREOISOMERISM; VINYL COMPOUNDS;

EID: 78650903885     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101504e     Document Type: Article

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