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Volumn , Issue 6, 1998, Pages 1027-1038

Chiral phosphinamides: New catalysts for the asymmetric reduction of ketones by borane

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EID: 33748621482     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a709174e     Document Type: Article
Times cited : (51)

References (41)
  • 1
    • 0003400107 scopus 로고
    • John Wiley and Sons Ltd., New York
    • For excellent recent surveys in asymmetric catalysis see (a) R. Noyori, Asymmetric Catalysis in Organic Synthesis, John Wiley and Sons Ltd., New York, 1994;
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 2
    • 0003544583 scopus 로고
    • ed. I. Ojima, VCH Press, Berlin
    • (b) Catalytic Asymmetric Synthesis, ed. I. Ojima, VCH Press, Berlin, 1993;
    • (1993) Catalytic Asymmetric Synthesis
  • 4
    • 33748620903 scopus 로고    scopus 로고
    • Hydrogenation of compounds containing C=C, C=O and C=N bonds
    • in the series, edited by S. Patai, The Chemistry of Double-Bonded Functional Groups Part 1, ch. 15
    • Hydrogenation of compounds containing C=C, C=O and C=N bonds, by M. Wills, in the series Chemistry of the Functional Groups, edited by S. Patai, Supplement A3: The Chemistry of Double-Bonded Functional Groups Part 1, ch. 15, pp. 781-842.
    • Chemistry of the Functional Groups , Issue.SUPPL. A3 , pp. 781-842
    • Wills, M.1
  • 28
    • 0001624426 scopus 로고
    • The oxazaphospholidine ring opening reaction of related compounds has been reported to proceed with retention of configuration at phosphorus, for example: J. M. Brown, J. V. Carey and M. J. H. Russell, Tetrahedron, 1990, 46, 4877.
    • (1990) Tetrahedron , vol.46 , pp. 4877
    • Brown, J.M.1    Carey, J.V.2    Russell, M.J.H.3
  • 31
    • 33748597922 scopus 로고    scopus 로고
    • note
    • The reaction between prolinol and diphenylphosphine chloride, in the presence of triethylamine and in dichloromethane solvent gave a large quantity of O-phosphinylated material. However the same reaction using diphenylprolinol gave mainly the N-phosphinylated product in 56% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.