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Volumn 351, Issue 9, 2009, Pages 1423-1430

Asymmetrie hydrogenation of α,ß-unsaturated esterphosphonates

Author keywords

Asymmetric hydrog nation; Homogeneous catalysis; Phosphonates; Rhodium

Indexed keywords


EID: 67649097697     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200900051     Document Type: Article
Times cited : (16)

References (31)
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    • Biomedical Chemistry, Applying Chemical Principles to the Understanding and Treatment of Disease, (Ed. : P. F. Torrence), Wiley, New York, 2000, pp 195-199.
    • Biomedical Chemistry, Applying Chemical Principles to the Understanding and Treatment of Disease, (Ed. : P. F. Torrence), Wiley, New York, 2000, pp 195-199.
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    • 0033520336 scopus 로고    scopus 로고
    • H. Jomaa, J. Wiesner, B. Sanderbrand, B. Altincicek, C. Weidemeyer, M. Hintz, I. Türbachova, M. Eberl, J. Zeidler, H. K. Lichtenthaler, D. Soldati, E. Beck, Science 1999, 285, 1573. 1-Deoxy-D-xylulose 5-phosphate reducto-isomerase is a key enzyme of the DOXP/MEP pathway of isoprenoid biosynthesis present in protozoans but not in mammals.
    • H. Jomaa, J. Wiesner, B. Sanderbrand, B. Altincicek, C. Weidemeyer, M. Hintz, I. Türbachova, M. Eberl, J. Zeidler, H. K. Lichtenthaler, D. Soldati, E. Beck, Science 1999, 285, 1573. 1-Deoxy-D-xylulose 5-phosphate reducto-isomerase is a key enzyme of the DOXP/MEP pathway of isoprenoid biosynthesis present in protozoans but not in mammals.
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    • Eds, J. G. de Vries, C. J. Elsevier, Wiley-VCH, New York
    • Handbook of Homogeneous Hydrogenation, (Eds.: J. G. de Vries, C. J. Elsevier), Wiley-VCH, New York, 2007.
    • (2007) Handbook of Homogeneous Hydrogenation
  • 15
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    • In a more recent paper the unexpected conjugated ethyl transfer from diethylaluminum chloride to a chiral enantiopure 3-phosphonopropenoyl derivative was reported, with unknown diastereoselectivity;
    • a) S. Gardner, M. Motevalli, K. Shastri, A. C. Sullivan, P. B. Wyatt, New. J. Chem. 2002, 26, 433. In a more recent paper the unexpected conjugated ethyl transfer from diethylaluminum chloride to a chiral enantiopure 3-phosphonopropenoyl derivative was reported, with unknown diastereoselectivity;
    • (2002) New. J. Chem , vol.26 , pp. 433
    • Gardner, S.1    Motevalli, M.2    Shastri, K.3    Sullivan, A.C.4    Wyatt, P.B.5
  • 18
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    • BPPM=N-tert-butoxycarbonyl-2-diphenylphoshino-4- methylene-diphenylphosphino pyrrolidine. Hydrogenation of the isomeric vinyl phosphonate gave 98% ee, for the use of a different catalyst in this reaction see
    • a) R. Kadyrov, R. Selke, R. Giernoth, J. Bargon, Synthesis 1999, 1056-1062. BPPM=N-tert-butoxycarbonyl-2-diphenylphoshino-4- methylene-diphenylphosphino pyrrolidine. Hydrogenation of the isomeric vinyl phosphonate gave 98% ee, for the use of a different catalyst in this reaction see
    • (1999) Synthesis , pp. 1056-1062
    • Kadyrov, R.1    Selke, R.2    Giernoth, R.3    Bargon, J.4
  • 22
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    • 2 substituent.
    • 2 substituent.
  • 23
    • 38049033351 scopus 로고    scopus 로고
    • For asymmetric hydrogenation using monodentate phosphoramidite ligands, see: a
    • For asymmetric hydrogenation using monodentate phosphoramidite ligands, see: a) A. J. Minnaard, B. L. Feringa, L. Lefort, J. G. de Vries, Acc. Chem. Res. 2007, 40, 1267;
    • (2007) Acc. Chem. Res , vol.40 , pp. 1267
    • Minnaard, A.J.1    Feringa, B.L.2    Lefort, L.3    de Vries, J.G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.