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Propargylic Trifluoromethyl Groups

Other functional groups tolerated in these isomerizations are ethers [65], alcohols [38, 66-69], propargylic trifluoromethyl groups [70], conjugated enones such as 36 [71] and esters [72] (Scheme 1.14). [Pg.1161]

Bis(trifluoromethyl)-4,5-difluoro-l,3-dioxole represents the monomer of a new family of amorphous fluoropoiymers (Teflon AF, DuPont) with unusual properties [89JFC(45)100]. Novel fluorinated 2,2-bis(triflu-oromethyl)dioxolanes containing alkyne groups have been synthesized from hexafluoroacetone and propargylic alcohol, bromomethyloxirane, or 1,2-bis(bromomethyl)oxirane [90MI1 91JFC(52)I59] (Scheme 95). [Pg.47]

See other pages where Propargylic Trifluoromethyl Groups is mentioned: [Pg.9]    [Pg.9]    [Pg.169]    [Pg.176]    [Pg.214]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.222]    [Pg.9]    [Pg.9]    [Pg.169]    [Pg.176]    [Pg.214]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.222]    [Pg.552]    [Pg.106]    [Pg.401]    [Pg.131]    [Pg.12]    [Pg.36]    [Pg.401]    [Pg.226]    [Pg.346]    [Pg.254]    [Pg.105]    [Pg.799]   


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Allylic and Propargylic Trifluoromethyl Groups

Propargyl groups

Trifluoromethyl group

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