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Thioacyl halides thiols

Thioacylation of Thiols with Thioacyl Halides, Thioacyl Anhydrides and Thioketenes... [Pg.435]

Thioacyl halides are not easily accessible. Aliphatic derivatives, in particular, can only be isolated in rare cases. Thioacylations of alcohols are therefore less important as synthetic methods than acylation of thiols with acyl hdides. Nevertheless, a variety of 0-alkyl and 0-aryl arenecarbothioates (2) have been obtained according to equation (4i).6.i4,25,2s... [Pg.448]

Thioacyl halides react with thiols in the presence of base and high yields of alkyl or aryl dithiocarbox-ylates (3) are obtained according to equation (57). ... [Pg.453]

In general, thiocarbonyl halides (59) function as thioacylation reagents with a variety of nucleophiles to yield the appropriate thio derivatives (60) (Scheme 31). For example, (59) on condensation with thiols, amines, potassium cyanide or potassium thiocyanide yields the corresponding thio compounds (60). Thiolocarboxylic acids (50) characteristically acylate alcohols and amines with desulfuration (Scheme 32). Dithiocarboxylic acid esters (54b) react with organolithium or Grignard reagents to give the dithioketals (61) after treatment with an alkyl halide (Scheme 33). [Pg.137]


See other pages where Thioacyl halides thiols is mentioned: [Pg.671]    [Pg.463]    [Pg.541]    [Pg.166]    [Pg.84]   
See also in sourсe #XX -- [ Pg.6 , Pg.453 ]

See also in sourсe #XX -- [ Pg.6 , Pg.453 ]




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