Vanadium-catalyzed oxidation of fert-butyl N-hydroxycarbamate to tert-butyl nitrosoformate and its Diels-Alder reaction with simple and functionalized dienes

Synlett

Volumn 23, Issue 16, 2012, Pages 2375-2380

  Hoshino, Yujiro ^a   Suzuki, Kenzo ^a   Honda, Kiyoshi ^a  

^a YOKOHAMA NATIONAL UNIVERSITY   (Japan)

Author keywords

Catalysis; Functionalized dienes; Nitroso Diels Alder reaction; Oxidation; Vanadium catalyst

Indexed keywords

ALKADIENE; CHEMICAL COMPOUND; HYDROGEN PEROXIDE; HYDROXAMIC ACID; N TERT BUTOXYCARBONYL 2 OXA 2 AZABICYCLO[2.2.1]HEPT 5 ENE; N TERT BUTOXYCARBONYL 2 OXA 3 AZABICYCLO[2.2.2]OCT 5 ENE; N TERT BUTOXYCARBONYL 3 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 6 METHOXYCARBONYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 3 [(TRIISOPROPYLSILYLOXY)METHYL] 6 METHOXYCARBONYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 3 HYDROXYMETHYL 6 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 3,6 DIPHENYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 4 (4 METHYL PENT 3 ENYL) 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 4 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 5 (4 METHYLPENT 3 ENYL) 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 5 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 (N' METHOXY N' METHYLCARBAMOYL) 3 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 CARBOXY 3 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 ETHOXYCARBOXY 3 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 HYDROXYMETHYL 3 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 METHOXYCARBOXY 3 HYDROXYMETHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; N TERT BUTOXYCARBONYL 6 METHOXYCARBOXY 3 METHYL 3,6 DIHYDRO 2H 1,2 OXAZINE; TERT BUTYL HYDROPEROXIDE; TERT BUTYL N HYDROXYCARBAMATE; TERT BUTYL NITROSOFORMATE; UNCLASSIFIED DRUG; VANADIUM;

ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIELS ALDER REACTION; EPOXIDATION; OXIDATION; REACTION OPTIMIZATION; ROOM TEMPERATURE; STEREOISOMERISM; STOICHIOMETRY;

EID: 84879031867     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0032-1317148     Document Type: Article

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