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First isolation of 1,3,2-dithiaphosphetane 2-sulfide
Authors:Hideaki Oshida  Juzo Nakayama
Affiliation:Department of Chemistry, Faculty of Science, Saitama University, Sakura-ku, Saitama 338-8570, Japan
Abstract:The treatment of tert-alkyl phenyl thioketones with Lawesson’s reagent (LR) gave two diastereomeric 1,3,2-dithiaphosphetane 2-sulfides in high yields. The structure of one of the major diastereomers was determined by X-ray crystallography. The reaction of 2-adamantanethione with LR yielded the corresponding spiro-1,3,2-dithiaphosphetane 2-sulfide derivative in 87% yield.
Keywords:Thioketone   Lawesson&rsquo  s reagent   1,3,2-Dithiaphosphetane 2-sulfide   X-ray analysis   Thermolysis
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