CuI-catalyzed aerobic oxidative α-aminaton cyclization of ketones to access aryl or alkenyl-substituted imidazoheterocycles

Journal of Organic Chemistry

Volumn 78, Issue 24, 2013, Pages 12494-12504

  Zhang, Yuhong ^a,b   Zhang, Yuanfei ^a   Chen, Zhengkai ^b   Wu, Wenliang ^a   Su, Weiping ^a  

^a FUJIAN INSTITUTE OF RESEARCH ON THE STRUCTURE OF MATTER   (China)

^b ZHEJIANG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GRAM SCALE; HYDROGEN ATOMS; MECHANISTIC STUDIES; MOST LIKELY; UNSATURATED KETONES;

ATOMS; CATALYSIS; FUNCTIONAL GROUPS; KETONES;

CYCLIZATION;

1 [2 (4 CHLOROPHENYL)IMIDAZO(1,2 A)PYRIDIN 3 YL]BUTAN 2 ONE; 2 (2 METHOXYPHENYL)IMIDAZO[1,2 A]PYRIDINE; 2 (4 IODOPHENYL)IMIDAZO[1,2 A]PYRIDINE; 2 (BENZOFURAN 2 YL)IMIDAZO[1,2 A]PYRIDINE; 2 (NAPHTHALEN 2 YL)IMIDAZO[1,2 A]PYRIDINE; 2 (THIOPHEN 2 YL)IMIDAZO[1,2 A]PYRIDINE; 2 [4 (METHYLSULFONYL)PHENYL]IMIDAZO[1,2 A]PYRIDINE; 2 [4 (METHYLSULFONYL)PHENYL]IMIDAZO[1,2 A]PYRIMIDINE; 2 [4 (TRIFLUOROMETHYL)PHENYL]IMIDAZO[1,2 A]PYRIDINE; 2 [IMIDAZO(1,2 A)PYRIDIN 2 YL]THIAZOLE; 2 AMINOPYRIDINE; 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 2 PHENYLIMIDAZO[2,1 A]ISOQUINOLINE; 3 ETHYL 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 3 METHYL 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 4 [IMIDAZO91,2 A)PYRIDIN 2 YL]BENZONITRILE; 6 BROMO 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 6 CHLORO 2 (4 CHLOROPHENYL)IMIDAZO[1,2 A]PYRIDINE; 6 METHYL 2 P TOLYLIMIDAZO[1,2 A]PYRIDINE; 6 PHENYLIMIDAZO[2,1 B]THIAZOLE; 7 METHOXY 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 7 METHYL 6 NITRO 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; 8 METHYL 2 PHENYLIMIDAZO[1,2 A]PYRIDINE; ACETOPHENONE; COPPER DERIVATIVE; KETONE DERIVATIVE; METHYL 4 [IMIDAZO(1,2 A)PYRIDIN 2 YL]BENZOATE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; ZOLIMIDINE;

AEROBIC METABOLISM; ARTICLE; CATALYST; CHEMICAL REACTION; CYCLIZATION; DRUG SYNTHESIS; ORTOLEVA KING REACTION; REACTION OPTIMIZATION;

CATALYSIS; COPPER; CYCLIZATION; HETEROCYCLIC COMPOUNDS; IMIDAZOLES; IODIDES; KETONES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION;

EID: 84890893691     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402134x     Document Type: Article

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