메뉴 건너뛰기




Volumn 9, Issue 18, 2007, Pages 3699-3701

Enantioselective imidazole-directed allylation of aldimines and ketimines

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALLYL COMPOUND; ALLYLCHLOROSILANE; IMIDAZOLE DERIVATIVE; IMINE; KETONE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34548526596     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol701723w     Document Type: Article
Times cited : (36)

References (17)
  • 6
    • 27944492745 scopus 로고    scopus 로고
    • For a recent and comprehensive review of asymmetric imine allylation methods, see
    • For a recent and comprehensive review of asymmetric imine allylation methods, see: Ding, H.; Friestad, G. K. Synthesis 2005, 2815.
    • (2005) Synthesis , pp. 2815
    • Ding, H.1    Friestad, G.K.2
  • 7
    • 33746256480 scopus 로고    scopus 로고
    • We have recently shown in two different contexts that phenols are effective activators of our allylchlorosilane family of reagents: (a) Burns, N. Z, Hackman, B. M, Ng, P. Y, Powelson, I. A, Leighton, J. L. Angew. Chem, Int. Ed. 2006, 45, 3811
    • We have recently shown in two different contexts that phenols are effective activators of our allylchlorosilane family of reagents: (a) Burns, N. Z.; Hackman, B. M.; Ng, P. Y.; Powelson, I. A.; Leighton, J. L. Angew. Chem., Int. Ed. 2006, 45, 3811.
  • 9
    • 34548544094 scopus 로고    scopus 로고
    • As is the case with allylsilane 1, 4 is produced, isolated, and employed as a ∼2:1 mixture of diastereomers. See the Supporting Information
    • As is the case with allylsilane 1, 4 is produced, isolated, and employed as a ∼2:1 mixture of diastereomers. See the Supporting Information.
  • 10
    • 33751500827 scopus 로고
    • For other recent advances in asymmetric ketimine allylation, see: a
    • For other recent advances in asymmetric ketimine allylation, see: (a) Hua, D. H.; Miao, S. W.; Chen, J. S.; Iguchi, S. J. Org. Chem. 1991, 56, 4.
    • (1991) J. Org. Chem , vol.56 , pp. 4
    • Hua, D.H.1    Miao, S.W.2    Chen, J.S.3    Iguchi, S.4
  • 15
    • 0035829093 scopus 로고    scopus 로고
    • Structurally related tertiary carbinamines have been accessed with, in some cases, very good diastereoselectivity employing the Ellman tert-butanesulfinimine methodology. See
    • Structurally related tertiary carbinamines have been accessed with, in some cases, very good diastereoselectivity employing the Ellman tert-butanesulfinimine methodology. See: Shaw, A. W.; deSolms, S. J. Tetrahedron Lett. 2001, 42, 7173.
    • (2001) Tetrahedron Lett , vol.42 , pp. 7173
    • Shaw, A.W.1    deSolms, S.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.