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Volumn 48, Issue 43, 2009, Pages 8078-8081

Copper-catalyzed C-C bond formation through C-H functionalization: Synthesis of multisubstituted indoles from N-aryl enaminones

Author keywords

C C coupling; Copper; Heterogeneous catalysis; Indoles; Synthesis design

Indexed keywords

C-C BOND FORMATION; C-C COUPLING; C-H FUNCTIONALIZATION; ENAMINONES; HETEROGENEOUS CATALYSIS; HIGH YIELD; INDOLES; PHENANTHROLINES; PRIMARY AMINES; SYNTHESIS DESIGN;

EID: 70349976206     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200902440     Document Type: Article
Times cited : (307)

References (54)
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    • Recently, a synthesis of indoles from N-aryl enamines in the absence of transition metals, via oxidative C-C bond formation mediated by phenyliodine(III) diacetate, has been reported
    • Recently, a synthesis of indoles from N-aryl enamines in the absence of transition metals, via oxidative C-C bond formation mediated by phenyliodine(III) diacetate, has been reported: W Yu, Y Du, K. Zhao, Org. Lett. 2009, 11, 2417-2420.
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    • See the Supporting Information for data and more experimental details.
    • See the Supporting Information for data and more experimental details.
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    • See the Supporting Information for measurement of the deuterium isotope effect.
    • See the Supporting Information for measurement of the deuterium isotope effect.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.