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Volumn , Issue 7, 1999, Pages 571-572

2,6-di-tert-butyl-4-diarylmethylene-2,5-cyclohexadiene-1-thiones. First isolable unannelated thioquinone methides

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EID: 0033245453     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1999.571     Document Type: Article
Times cited : (7)

References (20)
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    • ed by S. Oae, Plenum Press, New York, N. Y.
    • E. Campaigne, in "The Chemistry of the Carbonyl Group", ed. by S. Patai, Interscience Publ., New York, N. Y.(1966), p. 917; A. Ohno, in "Organic Chemistry of Sulfur", ed by S. Oae, Plenum Press, New York, N. Y.(1977), p. 189; F. Duss, in "Comprehensive Organic Chemistry", ed by D. N. Jones, Pergamon Press (1979), Vol. 3, p. 374.
    • (1977) Organic Chemistry of Sulfur , pp. 189
    • Ohno, A.1
  • 7
    • 0000840877 scopus 로고
    • ed by D. N. Jones, Pergamon Press
    • E. Campaigne, in "The Chemistry of the Carbonyl Group", ed. by S. Patai, Interscience Publ., New York, N. Y.(1966), p. 917; A. Ohno, in "Organic Chemistry of Sulfur", ed by S. Oae, Plenum Press, New York, N. Y.(1977), p. 189; F. Duss, in "Comprehensive Organic Chemistry", ed by D. N. Jones, Pergamon Press (1979), Vol. 3, p. 374.
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    • H. Bock, S. Mohmand, T. Hirabayashi, G. Maier, and H. P. Reisenauer, Chem. Ber., 116, 273 (1983); M. S. Raasch, J. Org. Chem., 44, 632 (1979).
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    • Raasch, M.S.1
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    • note
    • 3)δ 192.31, 149.69, 140.04, 132.78, 126.35, 37.00, 30.84.
  • 15
    • 0032563818 scopus 로고    scopus 로고
    • 4 was also effective for our recent dehydrative synthesis of acid-sensitive tetra(2-thienyl)allene; H. Kurata, M. Monden, T. Kawase, and M. Oda, Tetrahedron Lett., 39, 7135 (1998).
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7135
    • Kurata, H.1    Monden, M.2    Kawase, T.3    Oda, M.4
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    • and references therein
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    • (1956) Liebigs Ann. Chem. , vol.599 , pp. 131
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    • 15 15 W. Rundel, Chem. Ber., 101, 2956 (1968).
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    • Rundel, W.1


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