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Sulphenates allenic

Reaction of alkynols 156 with benzenesulphenyl chloride afforded either the vinylacety-lene sulphoxides 157 or the allene sulphoxides 158 depending upon the substitution pattern of alkynols 156. Vinylacetylene sulphoxides 157 result from a [2,3]-allylic rearrangement of the sulphenate ester 159 (equation 88). In the case of the cyclic... [Pg.272]

Rearrangement of acetylenic sulphenates to the allenic sulphoxides 151 was discovered when the synthesis of propargylic ester of trichloromethanesulphenic acid 152 was attempted (equation 86). This reaction is of general scope and gives very good yields of allenic sulphoxides (Table 14) from structurally diverse cohols and various sulphenyl chlorides Reaction of alkynols 153 with benzenesulphenyl chloride in the presence... [Pg.272]

The 5>>n-elimination of sulphenic and selenenic acids from unsaturated sulphoxides and selenoxides introduces a further site of unsaturation, examples being the addition of allyl alcohols to allenic sulphoxides to give ff-(allyloxy)vinyl sulphoxides... [Pg.55]


See other pages where Sulphenates allenic is mentioned: [Pg.1196]    [Pg.1204]    [Pg.66]    [Pg.38]    [Pg.75]    [Pg.1196]    [Pg.1204]    [Pg.66]    [Pg.38]    [Pg.75]    [Pg.272]    [Pg.272]    [Pg.313]    [Pg.56]    [Pg.39]   
See also in sourсe #XX -- [ Pg.739 ]




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