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Volumn 18, Issue 6, 2007, Pages 705-709

Enantioselective hydrosilylation of ketimines catalyzed by Lewis basic C2-symmetric chiral tetraamide

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; IMINE; LEWIS BASE; PROLINE DERIVATIVE;

EID: 34247138259     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.03.008     Document Type: Article
Times cited : (51)

References (18)
  • 13
    • 33846289229 scopus 로고    scopus 로고
    • For the other types of Lewis base organocatalysts for the asymmetric hydrosilylation of imines, see:
    • For the other types of Lewis base organocatalysts for the asymmetric hydrosilylation of imines, see:. Pei D., Wang Z., Wei S., and Sun J. Org. Lett. 8 (2006) 5913
    • (2006) Org. Lett. , vol.8 , pp. 5913
    • Pei, D.1    Wang, Z.2    Wei, S.3    Sun, J.4
  • 16
    • 33751096972 scopus 로고    scopus 로고
    • 2-symmetric chiral tetraamide was reported to behave as a stoichiometric Lewis basic activator for the allylation of imines, see:
    • 2-symmetric chiral tetraamide was reported to behave as a stoichiometric Lewis basic activator for the allylation of imines, see:. Jagtap S.B., and Tsogoeva S.B. Chem. Commun. (2006) 4747
    • (2006) Chem. Commun. , pp. 4747
    • Jagtap, S.B.1    Tsogoeva, S.B.2
  • 17
    • 0035903690 scopus 로고    scopus 로고
    • Heptacoordinate silicon structures have been previously reported, see examples:
    • Heptacoordinate silicon structures have been previously reported, see examples:. Kano N., Nakagawa N., and Kawashima T. Angew. Chem., Int. Ed. 40 (2001) 3450
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3450
    • Kano, N.1    Nakagawa, N.2    Kawashima, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.