The Basic Isomerization of Allyl Aryl Sulfides to Propenyl Aryl Sulfides1a
DS Tarbell, MA McCall
Index: Tarbell; McCall Journal of the American Chemical Society, 1952 , vol. 74, p. 48,53
Full Text: HTML
Citation Number: 69
Abstract
A series of allyl aryl sulfides has been shown to isomerize readily on treatment with base to the corresponding propenyl aryl sulfides. The structures have been established in most cases by catalytic reduction of both isomers to the n-propyl aryl sulfides, as well as by consideration of the infrared and ultraviolet spectra. The compounds studied are the allyl derivatives of thiodicylic and 3, 5-dichlorothiosalicylic acids, allyl 2-pyridyl sulfide and allyl ...
Related Articles:
The Synthesis of Some Alkamine Esters of Alkylthiobenzoic Acids
[Donleavy; English Journal of the American Chemical Society, 1940 , vol. 62, p. 220]
[Ratkovic, Zoran; Novakovic, Sladana B.; Bogdanovic, Goran A.; Segan, Dejan; Vukicevic, Rastko D. Polyhedron, 2010 , vol. 29, p. 2311 - 2317]
The metalation of some sulfur-containing organic compounds
[Gilman; Webb Journal of the American Chemical Society, 1949 , vol. 71, p. 4062,4063]