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Volumn 44, Issue 36, 2005, Pages 5882-5886

Facile synthesis of chiral α-difluoromethyl amines from N-(tert-butylsulfinyl)aldimines

Author keywords

Amines; Enantioselectivity; Fluorine; Sulfonamides; Synthetic methods

Indexed keywords

FLUORINE; SYNTHESIS (CHEMICAL);

EID: 24944543941     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200501769     Document Type: Article
Times cited : (143)

References (33)
  • 3
    • 24944544201 scopus 로고    scopus 로고
    • Fluorine in Drug Design: A Tutorial Review
    • (St Pete Beach, Florida, USA), January 9-14
    • J. R. McCarthy, Fluorine in Drug Design: A Tutorial Review, 17th Winter Fluorine Conference (St Pete Beach, Florida, USA), January 9-14, 2005.
    • (2005) 17th Winter Fluorine Conference
    • McCarthy, J.R.1
  • 8
    • 24944557435 scopus 로고    scopus 로고
    • note
    • 2OH) rather than a hydroxyl group (OH).
  • 27
    • 20344370237 scopus 로고    scopus 로고
    • - ion and different reaction conditions. See ref. [15], and for a recent report see: W. Xu, W. R. Dolbier, Jr., J. Org. Chem. 2005, 70, 4741.
    • (2005) J. Org. Chem. , vol.70 , pp. 4741
    • Xu, W.1    Dolbier Jr., W.R.2
  • 29
    • 0001650422 scopus 로고
    • N-(tert-butylsulfinyl)aldimine was chosen for its higher electrophilicity relative to normal unactivated imines and, more importantly, for its potential as a chiral auxiliary. For details about its preparation, see: a) K. Hovius, J. B. F. N. Engberts, Tetrahedron Lett. 1972, 13, 181;
    • (1972) Tetrahedron Lett. , vol.13 , pp. 181
    • Hovius, K.1    Engberts, J.B.F.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.