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Volumn 62, Issue 25, 1997, Pages 8693-8701

Structure and Thermal Decomposition of Some 5-(Cyclohexyloxy)thianthreniumyl Perchlorates

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EID: 0009526926     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970893m     Document Type: Article
Times cited : (8)

References (39)
  • 1
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    • Janssen, M. J., Ed.; Interscience Publishers: New York
    • (a) Shine, H. J. In Organosulfur Chemistry; Janssen, M. J., Ed.; Interscience Publishers: New York, 1967; pp 93-117.
    • (1967) Organosulfur Chemistry , pp. 93-117
    • Shine, H.J.1
  • 2
    • 3042939577 scopus 로고
    • ACS Symposium Series No. 69; Pryor, W. A., Ed.; American Chemical Society: Washington, D.C.
    • (b) Shine, H. J. In Organic Free Radicals; ACS Symposium Series No. 69; Pryor, W. A., Ed.; American Chemical Society: Washington, D.C., 1978; pp 359-375.
    • (1978) Organic Free Radicals , pp. 359-375
    • Shine, H.J.1
  • 4
    • 0009525316 scopus 로고
    • Stirling, C. J. M., Patai, S., Eds.; Wiley: New York
    • (d) Shine, H. J. In The Chemistry of the Sulfonium Group; Stirling, C. J. M., Patai, S., Eds.; Wiley: New York, 1981; pp 523-570.
    • (1981) The Chemistry of the Sulfonium Group , pp. 523-570
    • Shine, H.J.1
  • 9
    • 0343602930 scopus 로고
    • (a) Kim, K.; Shine, H. J. Tetrahedron Lett. 1974, 99. J. Org. Chem. 1974, 39, 2537.
    • (1974) J. Org. Chem. , vol.39 , pp. 2537
  • 12
    • 85034473635 scopus 로고    scopus 로고
    • Unpublished work of Dr. K. Kim
    • (a) Unpublished work of Dr. K. Kim.
  • 22
    • 0003737513 scopus 로고
    • Oxford University Press: Oxford
    • (a) For a discussion of this effect, see Sanders, J. K. M.; Hunter, B. K. Modern NMR Spectroscopy; Oxford University Press: Oxford, 1987; pp 299-302.
    • (1987) Modern NMR Spectroscopy , pp. 299-302
    • Sanders, J.K.M.1    Hunter, B.K.2
  • 23
    • 85034476790 scopus 로고    scopus 로고
    • note
    • (b) The same effect is seen in simpler 5-(alkyloxy)thianthreniumyl perchlorates in which the alkyl group has a stereogenic center attached to oxygen, such as 2-pentyl and 2-hexyl. The effect is absent where the alkyl group is, for example, methyl, ethyl, isopropyl. Unpublished work of W. Zhao.
  • 33
    • 85034471840 scopus 로고    scopus 로고
    • note
    • 25 Our assignments were confirmed, also, by the NMR data for 5j,k and by Ortep data not only for 5j, but also for the solid, trans,trans alcohol itself (see Figure 5 in the Supporting Information).
  • 35
    • 0347869828 scopus 로고
    • Li, S.; Allinger, N. L. Tetrahedron 1988, 44, 1339. The origin of the alcohols and the NMR solvent are not given.
    • (1988) Tetrahedron , vol.44 , pp. 1339
    • Li, S.1    Allinger, N.L.2
  • 39
    • 0004159483 scopus 로고
    • Oak Ridge National Laboratory, TN
    • Johnson, C. K. ORTEPII. Report ORNL-5138; 1976. Oak Ridge National Laboratory, TN.
    • (1976) ORTEPII. Report , vol.ORNL-5138
    • Johnson, C.K.1


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