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Volumn 132, Issue 18, 2010, Pages 6304-6305

A general strategy for regiocontrol in nickel-catalyzed reductive couplings of aldehydes and alkynes

Author keywords

[No Author keywords available]

Indexed keywords

CARBENE LIGANDS; CONJUGATED ENYNES; CYCLOPROPENYLIDENES; INTERNAL ALKYNES; N-HETEROCYCLIC CARBENE LIGANDS; REDUCTIVE COUPLINGS; REGIOCHEMICAL; REGIOCONTROL; SUBSTRATE BIAS; TERMINAL ALKYNE;

EID: 77953076639     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja102262v     Document Type: Article
Times cited : (140)

References (38)
  • 11
    • 77953076230 scopus 로고    scopus 로고
    • Many examples with aromatic, terminal, and silyl alkynes are described in ref 1. For ynamides
    • Many examples with aromatic, terminal, and silyl alkynes are described in ref 1. For ynamides
  • 17
    • 9644260362 scopus 로고    scopus 로고
    • For ligand-switchable directing effects
    • For ligand-switchable directing effects: Miller, K. M. and Jamison, T. F. J. Am. Chem. Soc. 2004, 126, 15342
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15342
    • Miller, K.M.1    Jamison, T.F.2
  • 26
    • 34447529183 scopus 로고    scopus 로고
    • For regioselectivity in imine-alkyne couplings
    • For regioselectivity in imine-alkyne couplings: Barchuk, A., Ngai, M. Y., and Krische, M. J. J. Am. Chem. Soc. 2007, 129, 8432
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 8432
    • Barchuk, A.1    Ngai, M.Y.2    Krische, M.J.3
  • 30
    • 77953074076 scopus 로고    scopus 로고
    • Ligand 5c is available as the racemate by the procedure employed
    • Ligand 5c is available as the racemate by the procedure employed.
  • 31
    • 33244482255 scopus 로고    scopus 로고
    • For development of the general structural motif
    • For development of the general structural motif: Funk, T. W., Berlin, J. M., and Grubbs, R. H. J. Am. Chem. Soc. 2006, 128, 1840
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1840
    • Funk, T.W.1    Berlin, J.M.2    Grubbs, R.H.3
  • 34
    • 33745350526 scopus 로고    scopus 로고
    • For alternate access to the 1,1-disubstituted isomer
    • For alternate access to the 1,1-disubstituted isomer: Takai, K., Sakamoto, S., Isshiki, T., and Kokumai, T. Tetrahedron 2006, 62, 7534
    • (2006) Tetrahedron , vol.62 , pp. 7534
    • Takai, K.1    Sakamoto, S.2    Isshiki, T.3    Kokumai, T.4
  • 35
    • 77953079031 scopus 로고    scopus 로고
    • For discussions of ligand size effects
    • For discussions of ligand size effects


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.