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Volumn , Issue 2, 1997, Pages 345-363

Enantioselective synthesis of α-phosphanyl ketones and 2-phosphanyl alcohols

Author keywords

2 Phosphanyl alcohols; Asymmetric synthesis; Asymmetric phosphanylation; Phosphane borane adducts; Phosphanyl hydrazones; Phosphanyl ketones

Indexed keywords


EID: 33748810344     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970212     Document Type: Article
Times cited : (21)

References (80)
  • 21
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    • [5a] G. Wilke, Angew. Chem. 1988, 100, 189-211;
    • (1988) Angew. Chem. , vol.100 , pp. 189-211
    • Wilke, G.1
  • 23
    • 0000277397 scopus 로고
    • [5b] W. Keim, Angew. Chem. 1990, 102, 251-260;
    • (1990) Angew. Chem. , vol.102 , pp. 251-260
    • Keim, W.1
  • 55
    • 0000434949 scopus 로고
    • (Ed.: J. D. Morrison), Academic Press, Orlando
    • [21b] D. Enders, in Asymmetric Synthesis (Ed.: J. D. Morrison), Academic Press, Orlando 1984, Vol. 3, 275-339.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 275-339
    • Enders, D.1
  • 67
    • 33748839118 scopus 로고    scopus 로고
    • note
    • -3. Further details on the crystal structure investigations are available on request from the Fachinformationszentrum Karlsruhe, Gesellschaft für wissenschaftlich-technische Information mbH, D-76344 Eggenstein-Leopoldshafen, on quoting the depository number CSD-406005, the names of the authors and the journal citation.
  • 68
    • 0003655672 scopus 로고
    • (Ed.: S. R. Hall, H. D. Flack, J. M. Stewart, Universities of Western Australia, Geneva and Maryland), Lamb, Perth
    • [27b] XTAL3.2 Reference Manual (Ed.: S. R. Hall, H. D. Flack, J. M. Stewart, Universities of Western Australia, Geneva and Maryland), Lamb, Perth, 1992.
    • (1992) XTAL3.2 Reference Manual
  • 69
    • 33748836265 scopus 로고    scopus 로고
    • note
    • 2 and subsequent chromatographic separation of the diastereomers.
  • 80
    • 33748842950 scopus 로고    scopus 로고
    • note
    • [1a,b] was deprotonated again with LDA, followed by alkylation with alkyl iodides and subsequent LAH reduction to afford the alcohols 13 as racemic mixtures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.