Access to C4-Functionalized Quinolines via Copper-Catalyzed Tandem Annulation of Alkynyl Imines with Diazo Compounds

Journal of Organic Chemistry

Volumn 81, Issue 17, 2016, Pages 7539-7544

  Zhu, Ruifeng ^a   Cheng, Guolin ^a   Jia, Chunqi ^a   Xue, Lulu ^a   Cui, Xiuling ^a  

^a HUAQIAO UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; COPPER;

COPPER CATALYZED; DIAZO COMPOUNDS; EFFICIENT SYNTHESIS; ELECTROCYCLIZATION; FUNCTIONALIZED; HIGH-EFFICIENCY; IN-SITU FORMATIONS; MILD REACTION CONDITIONS;

NITROGEN COMPOUNDS;

2 (6 ISOPROPYL 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; 2 (6 METHOXY 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; ALKYNYL GROUP; ALLENE DERIVATIVE; AZO COMPOUND; COPPER; DIAZO COMPOUND; FUNCTIONAL GROUP; IMINE; METHYL 2 (4 BROMOPHENYL) 2 (2 PHENYLQUINOLIN 4 YL)ACETATE; METHYL 2 (4 CHLOROPHENYL) 2 (2 PHENYLQUINOLIN 4 YL)ACETATE; METHYL 2 (4 FLUOROPHENYL) 2 (2 PHENYLQUINOLIN 4 YL)ACETATE; METHYL 2 (6 BROMO 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (6 CHLORO 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (6 FLUORO 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (6 METHYL 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (7 METHYL 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (8 CHLORO 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 (8 METHYL 2 PHENYLQUINOLIN 4 YL) 2 PHENYLACETATE; METHYL 2 PHENYL 2 (2 PHENYLQUINOLIN 4 YL)ACETATE; METHYL 2 PHENYL 2 [2 (3 TOLYL)QUINOLIN 4 YL]ACETATE; METHYL 2 PHENYL 2 [2 (4 TOLYL)QUINOLIN 4 YL]ACETATE; METHYL 2 PHENYL 2 [2 (THIOPHEN 2 YL)QUINOLIN 4 YL]ACETATE; METHYL 2 PHENYL 2 [2 PHENYL 6 (TRIFLUOROMETHYL)QUINOLIN 4 YL]ACETATE; METHYL 2 [2 (4 METHOXYPHENYL)QUINOLIN 4 YL] 2 PHENYLACETATE; METHYL 2 [2 (TERT BUTYL)QUINOLIN 4 YL] 2 PHENYLACETATE; METHYL 2 [2 [4 (TERTBUTYL)PHENYL]QUINOLIN 4 YL] 2 PHENYLACETATE; METHYL 2[2(4 CHLOROPHENYL)QUINOLIN 4 YLL] 2 PHENYLACETATE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANNULATION REACTION; ARTICLE; CHEMICAL REACTION; CYCLIZATION; DRUG SCREENING; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 84984904213     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.6b01227     Document Type: Article

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