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Volumn 20, Issue 11, 2014, Pages 3040-3044

Regio- and enantioselective synthesis of N-allylindoles by iridium-catalyzed allylic amination/transition-metal-catalyzed cyclization reactions

Author keywords

allylic substitution; asymmetric catalysis; enantioselectivity; iridium; N allylindole

Indexed keywords

ALLYLIC AMINATION; ALLYLIC SUBSTITUTION; ASYMMETRIC CATALYSIS; CATALYTIC AMOUNTS; CYCLIZATION REACTIONS; CYCLOOCTATETRAENE; ENANTIOSELECTIVE SYNTHESIS; N-ALLYLINDOLE;

EID: 84897609310     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201400026     Document Type: Article
Times cited : (37)

References (128)
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    • 2O, the same N-allylindole 5 ha was observed. For a similar CuI-mediated nitrogen cyclization onto alkynes with concurrent elimination of the TMS substituent, see.
    • 2O, the same N-allylindole 5 ha was observed. For a similar CuI-mediated nitrogen cyclization onto alkynes with concurrent elimination of the TMS substituent, see:, J. Ezquerra, C. Pedregal, C. Lamas, J. Barluenga, M. Pérez, M. A. García-Martín, J. M. González, J. Org. Chem. 1996, 61, 5804.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.