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Volumn 48, Issue 4, 2009, Pages 800-802

Efficient synthesis of chiral β-arylisopropylamines by using catalytic asymmetric hydrogenation

Author keywords

Drug design; Enamides; Enantioselectivity; Hydrogenation; Rhodium

Indexed keywords

CHEMICAL REACTIONS; ELECTRON TRANSITIONS; HYDROGENATION; RHODIUM; SYNTHESIS (CHEMICAL);

EID: 58249115089     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200805058     Document Type: Article
Times cited : (72)

References (48)
  • 1
    • 0003445429 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin
    • a) Comprehensive Asymmetric Catalysis I-III (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999;
    • (1999) Comprehensive Asymmetric Catalysis I-III
  • 3
    • 58249103940 scopus 로고    scopus 로고
    • Ed, I. Ojima, 2nd ed, Wiley-VCH, New York
    • c) Catalytic Asymmetric Synthesis (Ed.: I. Ojima), 2nd ed., Wiley-VCH, New York, 2000;
    • (2000) Catalytic Asymmetric Synthesis
  • 6
    • 15844427763 scopus 로고    scopus 로고
    • For representative references, see a
    • For representative references, see a) M. J. Burk, Y. M. Wang, J. R. Lee, J. Am. Chem. Soc. 1996, 118, 5142;
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 5142
    • Burk, M.J.1    Wang, Y.M.2    Lee, J.R.3
  • 35
    • 58249121671 scopus 로고    scopus 로고
    • Reference [3c];
    • a) Reference [3c];
  • 40
    • 0022921957 scopus 로고    scopus 로고
    • Notably, distinct reactivities of Z and E enamides were reported for Ru/binap-catalyzed (binap=2,2′-bis(diphenylphosphanyl)-1, 1′-binaphthyl) asymmetric hydrogenation of 1,2,3,4-tetrahydroisoquinoline derived enamides: whereas Z enamides were hydrogenated with excellent ee values, the corresponding E enamides showed no reactivity under the same hydrogenation conditions; see: a) R. Noyori, M. Ohta, Y. Hsiao, M. Kitamura, T. Ohta, H. Takaya, J. Am. Chem. Soc. 1986, 108, 7117;
    • Notably, distinct reactivities of Z and E enamides were reported for Ru/binap-catalyzed (binap=2,2′-bis(diphenylphosphanyl)-1, 1′-binaphthyl) asymmetric hydrogenation of 1,2,3,4-tetrahydroisoquinoline derived enamides: whereas Z enamides were hydrogenated with excellent ee values, the corresponding E enamides showed no reactivity under the same hydrogenation conditions; see: a) R. Noyori, M. Ohta, Y. Hsiao, M. Kitamura, T. Ohta, H. Takaya, J. Am. Chem. Soc. 1986, 108, 7117;
  • 42
    • 5344247907 scopus 로고    scopus 로고
    • For another asymmetric catalytic synthesis of this class of amines, see a
    • For another asymmetric catalytic synthesis of this class of amines, see a) I. A. Sayyed, A. Sudalai, Tetrahedron: Asymmetry 2004, 15, 3111;
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 3111
    • Sayyed, I.A.1    Sudalai, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.