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Volumn 73, Issue 5, 2008, Pages 1906-1910

Copper-catalyzed coupling of pyridines and quinolines with alkynes: A one-step, asymmetric route to functionalized heterocycles

Author keywords

[No Author keywords available]

Indexed keywords

FUNCTIONALIZED HETEROCYCLES;

EID: 41149135082     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702293h     Document Type: Article
Times cited : (134)

References (70)
  • 34
    • 0037157090 scopus 로고    scopus 로고
    • For the direct alkynylation of imines and related iminium salts, see: a
    • For the direct alkynylation of imines and related iminium salts, see: (a) Wei, C.; Li, C.-J. J. Am. Chem. Soc. 2002, 124, 5638.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 5638
    • Wei, C.1    Li, C.-J.2
  • 64
    • 41149164987 scopus 로고    scopus 로고
    • CuCl was employed rather than CuI as catalyst due to its higher solubility in this solvent mixture at low temperature
    • CuCl was employed rather than CuI as catalyst due to its higher solubility in this solvent mixture at low temperature.
  • 65
    • 0346243940 scopus 로고    scopus 로고
    • This ligand has been successfully employed by Knochel in the asymmetric alkynylation of N-alkyliminium salts. For example: Gommermann, N, Koradin, C, Polborn, K, Knochel P. Angew. Chem, Int. Ed. 2003, 42, 5763
    • This ligand has been successfully employed by Knochel in the asymmetric alkynylation of N-alkyliminium salts. For example: Gommermann, N.; Koradin, C.; Polborn, K.; Knochel P. Angew. Chem.. Int. Ed. 2003, 42, 5763.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.