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Volumn , Issue 22, 1997, Pages 3299-3313

1,5-Asymmetric induction of chirality: Highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of π-allyltricarbonyliron lactone complexes

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EID: 33748721622     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a704481j     Document Type: Article
Times cited : (38)

References (25)
  • 1
    • 0001180262 scopus 로고    scopus 로고
    • For a general review on π-allyltricarbonyliron lactone compounds including their synthesis and application to natural product chemistry see: S. V. Ley, L. R. Cox and G. Meek, Chem. Rev., 1996, 96, 423 and references cited therein.
    • (1996) Chem. Rev. , vol.96 , pp. 423
    • Ley, S.V.1    Cox, L.R.2    Meek, G.3
  • 2
    • 0000546031 scopus 로고
    • ed. 1. Fleming and B. M. Trost, Pergamon, Oxford
    • For a review on asymmetric epoxidation procedures see: R. A. Johnson and K. B. Sharpless, in Comprehensive Organic Synthesis, ed. 1. Fleming and B. M. Trost, Pergamon, Oxford, 1990, vol. 7, p. 389.
    • (1990) Comprehensive Organic Synthesis , vol.7 , pp. 389
    • Johnson, R.A.1    Sharpless, K.B.2
  • 4
    • 85088619969 scopus 로고
    • 4-dienetricarbonyliron complexes as chiral auxiliaries in asymmetric synthesis see: R. Grée, Synthesis, 1989, 353.
    • (1989) Synthesis , pp. 353
    • Grée, R.1
  • 11
    • 33748733026 scopus 로고    scopus 로고
    • Crystallographic analysis was performed in the Department of Chemistry, Cambridge by Drs A. Edwards and P. Raithby
    • Crystallographic analysis was performed in the Department of Chemistry, Cambridge by Drs A. Edwards and P. Raithby.
  • 12
    • 0001005278 scopus 로고
    • For the preparation and uses of organoaluminium reagents see: G. Zweifel and J. Miller, Org. React., 1984, 32, 375;
    • (1984) Org. React. , vol.32 , pp. 375
    • Zweifel, G.1    Miller, J.2
  • 13
    • 33748731475 scopus 로고
    • ed. I. Fleming and B. M. Trost, Pergamon, Oxford
    • J. Hauske, in Comprehensive Organic Synthesis, ed. I. Fleming and B. M. Trost, Pergamon, Oxford, 1990, vol. 1, p. 77.
    • (1990) Comprehensive Organic Synthesis , vol.1 , pp. 77
    • Hauske, J.1
  • 14
    • 33749106909 scopus 로고    scopus 로고
    • For an example of the use of a stereoselective reduction using triisobutylaluminium in natural product synthesis see: S. V. Ley and G. Meek, J. Chemn. Soc., Perkin Trans. 1, 1997, 1125.
    • (1997) J. Chemn. Soc., Perkin Trans. 1 , pp. 1125
    • Ley, S.V.1    Meek, G.2
  • 21
    • 33845557502 scopus 로고
    • Diethyl (2-oxo-2-phenylethyl)phosphonate was prepared via an Arbusov reaction. For a review of the Arbusov reaction see: A. Bhattacharya and G. Thyagarajan, Chem. Rev., 1981, 81, 415.
    • (1981) Chem. Rev. , vol.81 , pp. 415
    • Bhattacharya, A.1    Thyagarajan, G.2
  • 23
    • 0004150157 scopus 로고
    • University of Göttingen, Germany
    • G. M. Sheldrick, SHELXS-93, University of Göttingen, Germany, 1993.
    • (1993) SHELXS-93
    • Sheldrick, G.M.1
  • 24
    • 0004150157 scopus 로고
    • Siemens Analytical Instrumentation Inc., Madison, WI
    • G. M. Sheldrick, SHELXTL/PC version 5.03, Siemens Analytical Instrumentation Inc., Madison, WI, 1994.
    • (1994) SHELXTL/PC Version 5.03
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.