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Volumn 14, Issue 17, 2012, Pages 4658-4661

Ru(CO)-salen-catalyzed synthesis of enantiopure aziridinyl ketones and formal asymmetric synthesis of (+)-PD 128907

Author keywords

[No Author keywords available]

Indexed keywords

3,4,4A,10B TETRAHYDRO 4 PROPYL 2H,5H (1)BENZOPYRANO(4,3 B) 1,4 OXAZIN 9 OL; 3,4,4A,10B-TETRAHYDRO-4-PROPYL-2H,5H-(1)BENZOPYRANO(4,3-B)-1,4-OXAZIN-9-OL; AZIRIDINE DERIVATIVE; BENZOPYRAN DERIVATIVE; KETONE; ORGANOMETALLIC COMPOUND; OXAZINE DERIVATIVE; RUTHENIUM;

EID: 84866011243     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol302095r     Document Type: Article
Times cited : (46)

References (62)
  • 9
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    • (1999) Comprehensive Asymmetric Catalysis II , vol.2 , pp. 607
    • Jacobsen, E.N.1
  • 11
    • 1542296467 scopus 로고    scopus 로고
    • In; McCleverty, J. Elsevier: Oxford, Vol. Chap. 9.4
    • Katsuki, T. In Comprehensive Coodination Chemistry II; McCleverty, J., Ed.; Elsevier: Oxford, 2003; Vol. 9, Chap. 9.4, p 207.
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    • Katsuki, T.1
  • 17
    • 0033063570 scopus 로고    scopus 로고
    • Copper-mediated aziridination of acrolein has been reported, though nonenantioselectively
    • Copper-mediated aziridination of acrolein has been reported, though nonenantioselectively: Dauban, P.; Dodd, R. H. J. Org. Chem. 1999, 64, 5304
    • (1999) J. Org. Chem. , vol.64 , pp. 5304
    • Dauban, P.1    Dodd, R.H.2
  • 44
    • 33947334762 scopus 로고
    • For the first aziridination using azide compounds, see
    • For the first aziridination using azide compounds, see: Kwart, H.; Kahn, A. A. J. Am. Chem. Soc. 1967, 89, 1951
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 1951
    • Kwart, H.1    Kahn, A.A.2
  • 45
    • 0000072415 scopus 로고
    • Asymmetric aziridination using arenesulfonyl azide under irradiation has been reported
    • Asymmetric aziridination using arenesulfonyl azide under irradiation has been reported: Li, Z.; Quan, R. W.; Jacobsen, E. N. J. Am. Chem. Soc. 1995, 117, 5889
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5889
    • Li, Z.1    Quan, R.W.2    Jacobsen, E.N.3
  • 53
    • 0032770159 scopus 로고    scopus 로고
    • Complex 1 does not catalyze the hetero Diels-Alder reaction (unpublished result), though Ru(NO)-salen complexes do.
    • Complex 1 does not catalyze the hetero Diels-Alder reaction (unpublished result), though Ru(NO)-salen complexes do. Mihara, J.; Hamada, T.; Takeda, T.; Irie, R.; Katsuki, T. Synlett 1999, 1160
    • (1999) Synlett , pp. 1160
    • Mihara, J.1    Hamada, T.2    Takeda, T.3    Irie, R.4    Katsuki, T.5
  • 54
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    • CCDC 771523 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC 771523 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.
  • 61
    • 84876299742 scopus 로고    scopus 로고
    • 2/hexane gave a single crystal. The structure of 9 was confirmed to be R by X-ray analysis of the crystal. Accordingly, the configuration of 8 was determined to be R. CCDC 813702 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • 2/hexane gave a single crystal. The structure of 9 was confirmed to be R by X-ray analysis of the crystal. Accordingly, the configuration of 8 was determined to be R. CCDC 813702 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.