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Volumn 93, Issue 16, 1971, Pages 4063-4065

Geometry of the anti-Tricyclo[3.1.0.0]hexane and Cyclohexa-1,4-diene Systems

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EID: 0013490058     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00745a050     Document Type: Letter
Times cited : (16)

References (24)
  • 4
    • 33846231239 scopus 로고
    • photolysis of triphenylcyclopropene with a sensitizer provided a cyclopropylcyclopropene derivative in addition to a normal dimer (tricyclohexane)
    • C. Deboer and R. Breslow, Tetrahedron Lett., 1033 (1967); photolysis of triphenylcyclopropene with a sensitizer provided a cyclopropylcyclopropene derivative in addition to a normal dimer (tricyclohexane);
    • (1967) Tetrahedron Lett. , pp. 1033
    • Deboer, C.1    Breslow, R.2
  • 22
    • 0013445932 scopus 로고
    • 2,5]pent-3-yl p-bromo-benzoate, see ref 1c; (c)
    • 2,5]pent-3-yl p-bromo-benzoate, see ref 1c; (c) S. Masamune, Tetrahedron Lett., 945 (1965);
    • (1965) Tetrahedron Lett. , pp. 945
    • Masamune, S.1
  • 24
    • 85022682618 scopus 로고
    • In the cases of esters of exo-1,3-diphenylbicyclobutanecarboxylic acid, uv maxima are shifted to shorter wavelengths (ca. 220 nm) from the normal position (ca. 270 nm) apparently due to the steric hindrance between the carbethoxy and phenyl groups
    • J. M. Schulman and G. J. Fisanick, J. Amer. Chem. Soc., 92, 6654 (1970). In the cases of esters of exo-1,3-diphenylbicyclobutanecarboxylic acid, uv maxima are shifted to shorter wavelengths (ca. 220 nm) from the normal position (ca. 270 nm) apparently due to the steric hindrance between the carbethoxy and phenyl groups.
    • (1970) J. Amer. Chem. Soc. , vol.92 , pp. 6654
    • Schulman, J.M.1    Fisanick, G.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.