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Volumn 102, Issue 15, 1980, Pages 5077-5081

Stereoelectronic Effects in the Reactions of Epimeric 2-Aryloxy-2-oxy-1,3,2-dioxaphosphorinanes and Oxazaphosphorinanes

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EID: 0012820897     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00535a044     Document Type: Article
Times cited : (103)

References (49)
  • 25
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    • J. Am. Chem. Soc., 95, 4659 (1973);
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4659
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    • 1977
    • J. Org. Chem., 1977, 42, 1549 (1977).
    • (1977) J. Org. Chem. , vol.42 , pp. 1549
  • 28
    • 33947085951 scopus 로고
    • J. Am. Chem. Soc., 95, 4659 (1973);
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4659
  • 46
    • 33947093789 scopus 로고
    • in particular discuss the stereochemistry of reaction in a phosphorinane ring system.
    • M. Bauman and W. S. Wadsworth, Jr., J. Am. Chem. Soc., 100, 6388 (1978), in particular discuss the stereochemistry of reaction in a phosphorinane ring system.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 6388
    • Bauman, M.1    Wadsworth, W.S.2
  • 49
    • 85021547669 scopus 로고    scopus 로고
    • (* O. 2 kcal/mol) and ground-state energies (° O. 1 kcal/mol) for the epimeric tetracyclic phosphordiamidates 11. Again (R. Rowell, unpublished) the b isomer is in a boat-type conformation
    • This picture is supported by the near-equal rates of hydrolysis (* O. 2 kcal/mol) and ground-state energies (° O. 1 kcal/mol) for the epimeric tetracyclic phosphordiamidates 11. Again (R. Rowell, unpublished) the b isomer is in a boat-type conformation
    • This picture is supported by the near-equal rates of hydrolysis


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.