Vinylogous reactivity of enol diazoacetates with donor-acceptor substituted hydrazones. Synthesis of substituted pyrazole derivatives

Journal of Organic Chemistry

Volumn 78, Issue 4, 2013, Pages 1583-1588

  Xu, Xinfang ^a   Zavalij, Peter Y ^a   Hu, Wenhao ^b   Doyle, Michael P ^a  

^a University of Maryland   (United States)

^b EAST CHINA NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CASCADE PROCESS; DINITROGEN; DONOR-ACCEPTORS; HYDRAZONES; LEWIS ACID; NUCLEOPHILIC ADDITIONS; PYRAZOLE DERIVATIVES; REGIOSPECIFIC SYNTHESIS; VINYLOGOUS REACTIVITIES;

ADDITION REACTIONS; CATALYSIS;

CYCLIZATION;

AZO COMPOUND; DIAZOCARBONYL DERIVATIVE; DINITROGEN PENTOXIDE; ETHYL 1 (2,4 DICHLOROPHENYL) 5 (2 METHOXY 2 OXOETHYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 1 (4 CHLOROPHENYL) 5 (2 METHOXY 2 OXOETHYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 1 (4 CHLOROPHENYL) 5 (2 METHOXY 2 OXOETHYL) 4 METHYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 (2 METHOXY 2 OXOETHYL) 1 (4 METHOXYPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 (2 METHOXY 2 OXOETHYL) 1 (4 METHOXYPHENYL) 4 METHYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 (2 METHOXY 2 OXOETHYL) 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 (2 METHOXY 2 OXOETHYL) 1 (4 TOLYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 (2 METHOXY 2 OXOETHYL) 1 PHENYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 [2 (BENZYLOXY) 2 OXOETHYL] 1 (4 METHOXYPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 [2 (BENZYLOXY) 2 OXOETHYL] 1 (4 METHOXYPHENYL) 4 METHYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 [2 (BENZYLOXY) 2 OXOETHYL] 4 ETHYL 1 (4 METHOXYPHENYL) 4 METHYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 5 [2 (TERT BUTOXY) 2 OXOETHYL] 1 (4 METHOXYPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; HYDRAZONE DERIVATIVE; LEWIS ACID; PYRAZOLE DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG;

AROMATIZATION; ARTICLE; CATALYST; CYCLIZATION; ONE POT SYNTHESIS; STEREOCHEMISTRY; SUBSTITUTION REACTION;

AZO COMPOUNDS; CATALYSIS; CYCLIZATION; HYDRAZONES; MOLECULAR STRUCTURE; PYRAZOLES; STEREOISOMERISM;

EID: 84873957608     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo302696y     Document Type: Article

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