Method for the Synthesis of Phenothiazines via a Domino Iron-Catalyzed C-S/C-N Cross-Coupling Reaction

Journal of Organic Chemistry

Volumn 80, Issue 12, 2015, Pages 6128-6132

  Hu, Weiye ^a   Zhang, Songlin ^a  

^a SOOCHOW UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CATALYSTS; INSECTICIDES; IRON; REGIOSELECTIVITY;

COPPER CATALYST; CROSS COUPLING REACTIONS; ENVIRONMENTALLY BENIGN;

CHEMICAL REACTIONS;

10H PHENOTHIAZINE; 12H QUINOXALINO[2,3 B][1,4]BENZOTHIAZINE; 2 (TRIFLUOROMETHYL) 10H PHENOTHIAZINE; 2 CHLORO 10H PHENOTHIAZINE; 2 CHLORO 12H QUINOXALINO[2,3 B][1,4]BENZOTHIAZINE; 2 METHYL 10H PHENOTHIAZINE; 2,7 DICHLORO 10H PHENOTHIAZINE; 2,8 DICHLORO 10H PHENOTHIAZINE; 3 CHLORO 10H PHENOTHIAZINE; 3 METHYL 5H PYRIDO[2,3 B][1,4]BENZOTHIAZINE; 3 METHYL 7 CHLORO 5H PYRIDO[2,3 B][1,4]BENZOTHIAZINE; 5H PYRIDO[2,3 B][1,4]BENZOTHIAZINE; 7 CHLORO 5H PYRIDO[2,3 B][1,4]BENZOTHIAZINE; COPPER; IRON; PALLADIUM; PHENOTHIAZINE DERIVATIVE; UNCLASSIFIED DRUG; PHENOTHIAZINE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL PARAMETERS; CONTROLLED STUDY; CROSS COUPLING REACTION; DRUG SYNTHESIS; REACTION TIME; REGIOSELECTIVITY; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

CATALYSIS; COPPER; IRON; MOLECULAR STRUCTURE; PALLADIUM; PHENOTHIAZINES;

EID: 84934959055     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b00568     Document Type: Article

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