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Volumn 9, Issue 1, 1998, Pages 29-40

New consecutive photochemical reactions of naphtho[1,8-de]-1,3-dithiin-1-n-tosylsulfilimines via the through-space interaction between two sulfur atoms; A convenient method for preparation of N-tosylaldimines

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EID: 0013492245     PISSN: 10427163     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1071(1998)9:1<29::AID-HC4>3.0.CO;2-Y     Document Type: Article
Times cited : (4)

References (68)
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    • Other products were mainly 4 and 2,3-dimethyl-2-butenyl-naphtho[1,8-cd]-1,2-dithiole. Lewis acid catalyzed imino Diels-Alder reactions for Ref. [2]
    • Other products were mainly 4 and 2,3-dimethyl-2-butenyl-naphtho[1,8-cd]-1,2-dithiole. Lewis acid catalyzed imino Diels-Alder reactions for Ref. [2].
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    • Thermal Stevens-type rearrangement of sulfilimines: (a) H. Kise, G. F. Whitefield, D. Swern, J. Org. Chem., 37, 1972, 1125; (b) T. L. Gilchrist, C. J. Moody, C. W. Rees, J. Chem, Soc. Perkin Trans., 1, 1975, 1964; (c) M. Hori, T. Kataoka, H. Shimizu, K. Matsuo, Tetrahedron Lett., 1979, 3969; (d) Y. Tamura, S. M. Bayomi, C. Mukai, M. Ikeda, M. Murase, M. Kise, Tetrahedron Lett., 21, 1980, 553.
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    • Tamura, Y.1    Bayomi, S.M.2    Mukai, C.3    Ikeda, M.4    Murase, M.5    Kise, M.6


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