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Volumn 54, Issue 43, 1998, Pages 13155-13166

Correlation between optical rotation sign and conformation of γ- butyrolactones. An empirical correlation rule to predict optical activity and stereochemistry of γ-butyrolactones

Author keywords

[No Author keywords available]

Indexed keywords

BUTYRIC ACID DERIVATIVE; LACTONE DERIVATIVE;

EID: 0032558628     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00817-5     Document Type: Article
Times cited : (8)

References (49)
  • 1
    • 0004270233 scopus 로고
    • Mir Publishers: Moscow
    • 1. (a) Potapov, V. M. Stereochemistry, Mir Publishers: Moscow, 1978, pp. 200-207.
    • (1978) Stereochemistry , pp. 200-207
    • Potapov, V.M.1
  • 14
    • 37049063001 scopus 로고
    • For nontheoretical discussions, see: ref. 1d.
    • (d) Mason, S. F. Q. Rev. Chem. Soc. 1963, 17, 20. For nontheoretical discussions, see: ref. 1d.
    • (1963) Q. Rev. Chem. Soc. , vol.17 , pp. 20
    • Mason, S.F.1
  • 24
    • 0004226987 scopus 로고
    • Addison-Wesley: New York
    • 12. Loudon, G. M. Organic Chemistry, Addison-Wesley: New York, 1984, p. 255.
    • (1984) Organic Chemistry , pp. 255
    • Loudon, G.M.1
  • 47
    • 0001507630 scopus 로고
    • 26. This reaction condition was reported for the transformation of nitro compounds to carbonyl compounds. However in this case, the reaction converted compound 2 to compound 5 rather than compound 6. See: Kornblum, N.; Wade, P. A. J. Org. Chem. 1973, 38, 1418.
    • (1973) J. Org. Chem. , vol.38 , pp. 1418
    • Kornblum, N.1    Wade, P.A.2
  • 48
    • 0000125222 scopus 로고
    • 27. It should be noted that this is the first mild ozonation converting a nitro compound to a carbonyl compound, for previous ozonations proceeded under strict and inconvenient conditions, see: (a) McMurry, J. E.; Melton, J.; Padgett, H. J. Org. Chem. 1974, 39, 259.
    • (1974) J. Org. Chem. , vol.39 , pp. 259
    • McMurry, J.E.1    Melton, J.2    Padgett, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.