Chemistry of Heterocyclic Compounds p. 624 - 626 (1985)
Update date:2022-08-04
Topics: Experimental conditions Conversions Pummerer rearrangement Allyl aryl sulfoxides
Fedorov, N. V.
Shevchenko, M. V.
Anisimov, A. V.
Viktorova, E. A.
In the presence of acetic acid, allyl phenyl sulfoxides forms α-acetoxyallyl phenyl sulfides and 2-acetoxymethyl-2,3-dihydrobenzothiophene; under the same conditions allyl 1-naphthyl sulfoxide gives 2-methyl-2,3-dihydronaphtho-<1,2-b>thiophenoxide.
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Doi:10.1021/jm00153a004
(1986)Doi:10.1007/BF00951284
(1985)Doi:10.1021/jm070612v
(2007)Doi:10.1039/c8cc07781a
(2018)Doi:10.1021/ja01554a076
(1958)Doi:10.1016/0022-328X(85)80204-7
(1985)