메뉴 건너뛰기




Volumn 45, Issue 24, 2006, Pages 3909-3912

Chiral phosphoric acids: Powerful organocatalysts for asymmetric addition reactions to imines

Author keywords

Amines; Asymmetric synthesis; Enantioselectivity; Organocatalysis; Phosphorus

Indexed keywords

ADDITION REACTIONS; CATALYST ACTIVITY; NITROGEN COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 33746272976     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200600529     Document Type: Review
Times cited : (400)

References (55)
  • 3
    • 0002788460 scopus 로고
    • for the first organocatalytic asymmetric synthesis, see: c) G. Bredig, P. S. Fiske, Biochem. Z. 1912, 46, 7.
    • (1912) Biochem. Z. , vol.46 , pp. 7
    • Bredig, G.1    Fiske, P.S.2
  • 7
    • 33746303765 scopus 로고    scopus 로고
    • c) Acc. Chem. Res. 2004, 37(8).
    • (2004) Acc. Chem. Res. , vol.37 , Issue.8
  • 8
    • 0001329652 scopus 로고
    • For instructive discussions of general acid catalysis: a) W. P. Jencks, Chem. Rev. 1972, 72, 705;
    • (1972) Chem. Rev. , vol.72 , pp. 705
    • Jencks, W.P.1
  • 11
    • 33746277515 scopus 로고    scopus 로고
    • DOI: 10.1002/chem.200501076
    • Reviews: a) S. J. Connon, Chem. Eur. J. 2006, DOI: 10.1002/chem. 200501076;
    • (2006) Chem. Eur. J.
    • Connon, S.J.1
  • 18
    • 31544482203 scopus 로고    scopus 로고
    • For a discussion of the use of chiral Brønsted acid catalysts in conjunction with Lewis acids and other additives, see: H. Yamamoto, K. Futatsugi, Angew. Chem. 2005, 117, 1958;
    • (2005) Angew. Chem. , vol.117 , pp. 1958
    • Yamamoto, H.1    Futatsugi, K.2
  • 41
    • 4644355914 scopus 로고    scopus 로고
    • Shortly thereafter, analogues of 7a,b were shown to serve as highly effective promoters of both aza-Friedel-Crafts-type alkylation reactions of furan and imine hydrophosphonylations; see: a) D. Uraguchi, K. Sorimachi, M. Terada, J. Am. Chem. Soc. 2004, 126, 11804;
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 11804
    • Uraguchi, D.1    Sorimachi, K.2    Terada, M.3
  • 46
    • 33746182597 scopus 로고    scopus 로고
    • b) for a similar study, which includes an example of a prototype reductive amination protocol, see: S. Hoffmann, A. M. Seayad, B. List, Angew. Chem. 2005, 117, 7590;
    • (2005) Angew. Chem. , vol.117 , pp. 7590
    • Hoffmann, S.1    Seayad, A.M.2    List, B.3
  • 48
    • 31944452587 scopus 로고    scopus 로고
    • c) phosphoric acids have also been utilized recently in asymmetric Pictet-Spengler reactions: J. Seayad, A. M. Seayad, B. List, J. Am. Chem. Soc. 2006, 128, 1086;
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1086
    • Seayad, J.1    Seayad, A.M.2    List, B.3
  • 49
    • 33746297277 scopus 로고    scopus 로고
    • d) for a short review of organocatalytic asymmetric reduction of α,β-unsaturated aldehydes, see: H. Adolfsson, Angew. Chem. 2005, 117, 3404;
    • (2005) Angew. Chem. , vol.117 , pp. 3404
    • Adolfsson, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.