1987
DOI: 10.1002/chin.198712163
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ChemInform Abstract: Mechanistic Aspects and Profiles of the Double Elimination Reaction of β‐Substituted Sulfones.

Abstract: The β‐substituted sulfones (I), (V), and (X) react with tert‐butylate (II) to form the corresponding vinyl sulfones (III), (VI), and (XI).

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“…β-Hydroxysulfides are attractive tools in organic synthesis, which are actively used in the synthesis of allylic alcohols, cyclic sulfides, thioketones, and physiologically active compounds [1][2][3][4][5]. Products of their oxidation, β-hydroxysulfones, are useful reagents for preparation of lactones [6], 2,5disubstituted tetrahydrofuranes [7], and vinyl sulfones [8]. Compounds containing phenylsulfonyl fragment are also widely used in organic synthesis [9].…”
Section: Introductionmentioning
confidence: 99%
“…β-Hydroxysulfides are attractive tools in organic synthesis, which are actively used in the synthesis of allylic alcohols, cyclic sulfides, thioketones, and physiologically active compounds [1][2][3][4][5]. Products of their oxidation, β-hydroxysulfones, are useful reagents for preparation of lactones [6], 2,5disubstituted tetrahydrofuranes [7], and vinyl sulfones [8]. Compounds containing phenylsulfonyl fragment are also widely used in organic synthesis [9].…”
Section: Introductionmentioning
confidence: 99%