Potassium carbonate catalyzed regioselective aminohalogenation of β-nitrostyrenes by using benzyl carbamate/N-chlorosuccinimide as a new nitrogen/chlorine source

Synthesis

Volumn , Issue 22, 2011, Pages 3680-3686

  Ji, Xiaoyun ^a   Mei, Haibo ^a   Qian, Yu ^a   Han, Jianlin ^a   Li, Guigen ^a,c   Pan, Yi ^a,b  

^a NANJING UNIVERSITY   (China)

^b NANJING UNIVERSITY   (China)

^c TEXAS TECH UNIVERSITY   (United States)

Author keywords

alkenes; amides; aminations; carbamates; chlorinations

Indexed keywords

AMINATIONS; CARBAMATES; CHEMICAL YIELDS; HIGH EFFICIENCY; N-CHLOROSUCCINIMIDE; NITROSTYRENE; REGIO-SELECTIVE; ROOM TEMPERATURE;

AMIDES; CATALYSIS; CHLORINE; DICHLOROMETHANE; OLEFINS;

POTASSIUM;

BENZYL (2,2 DICHLORO 2 NITRO 1 PHENYLETHYL)CARBAMATE; BENZYL 2,2 [DICHLORO 1 (4 METHOXYPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [1 (2 BROMOPHENYL) 2,2 DICHLORO 2 NITROETHYL]CARBAMATE; BENZYL [1 (3 BROMO 4 METHOXYPHENYL) 2,2 DICHLORO NITROETHYL]CARBAMATE; BENZYL [1 (3 BROMOPHENYL) 2,2 DICHLORO 2 NITROETHYL]CARBAMATE; BENZYL [1 (4 BROMOPHENYL) 2,2 DICHLORO NITROETHYL]CARBAMATE; BENZYL [1 [2 (BENZYLOXY)PHENYL] 2,2 DICHLORO 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (2 CHLOROPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (2 METHOXYPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (3 CHLOROPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (3 FLUOROPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (4 CHLOROPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (4 CYANOPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (4 FLUOROPHENYL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 1 (NAPHTH 1 YL) 2 NITROETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 2 NITRO 1 (2 TOLYL)ETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 2 NITRO 1 (3 TOLYL)ETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 2 NITRO 1 (4 TOLYL)ETHYL]CARBAMATE; BENZYL [2,2 DICHLORO 2 NITRO 1 [4 (TRIFLUOROMETHYL)PHENYL]ETHYL]CARBAMATE; NITROSTYRENE DERIVATIVE; POTASSIUM CARBONATE; STYRENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHLORINATION; CONTROLLED STUDY; ELECTROPHILICITY; HALOGENATION; REACTION TIME; ROOM TEMPERATURE; SYNTHESIS;

EID: 80755153715     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260245     Document Type: Article

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