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Volumn 48, Issue 48, 2009, Pages 9135-9138

Asymmetric hydrogenation of quinoxalines with diphosphinite ligands: A practical synthesis of enantioenriched, substituted tetrahydroquinoxalines

Author keywords

Asymmetric catalysis; Diphosphinite ligands; Hydrogenation; Tetrahydroquinoxalines

Indexed keywords

ASYMMETRIC CATALYSIS; ASYMMETRIC HYDROGENATION; DIPHOSPHINITE LIGANDS; OPTICALLY ACTIVE; QUINOXALINES; SYNTHETIC APPROACH; TETRAHYDROQUINOXALINES;

EID: 70449591239     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200904518     Document Type: Article
Times cited : (139)

References (56)
  • 43
    • 33947721706 scopus 로고    scopus 로고
    • For selected examples of asymmetric hydrogenation of furans, see: a) S. Kaiser, S. P. Smidt, A. Pfaltz, Angew. Chem. 2006, 118, 5318;
    • (2006) Angew. Chem. , vol.118 , pp. 5318
    • Kaiser, S.1    Smidt, S.P.2    Pfaltz, A.3
  • 46
    • 21244463410 scopus 로고    scopus 로고
    • For selected examples of asymmetric hydrogenation of pyridines, see : a) C. Y. Legault, A. B. Charette, J. Am. Chem. Soc. 2005, 127, 8966;
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 8966
    • Legault, C.Y.1    Charette, A.B.2
  • 50
    • 70449586101 scopus 로고    scopus 로고
    • EP 803502
    • R. Fuchs, EP 803502, 1997.
    • (1997)
    • Fuchs, R.1
  • 55
    • 70449590618 scopus 로고    scopus 로고
    • CCDC 748584 (2o) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 748584 (2o) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 56
    • 70449575183 scopus 로고    scopus 로고
    • For details, see the Supporting Information.
    • For details, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.