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2- -2,5-alkadienoic acid 2-alkyn

Isomerizations. A convenient method for the conversion of alkynes to conjugated dienes is by treatment with Ph P. The synthetic application is shown in the preparation of 2,4-alkadienols from 2-alkynoic acids involving esterification with pentafluorophenol, isomerization with PhjP (PhMe, 50°), and reduction with DIBAL-H. Even propargyl bromide can be isomerized to give 1-bromopropadiene, albeit in 29% yield. Conjugated alkadienoic esters and amides are obtained in one step from the pentafluorophenyl alkynoates on reaction with alcohols and amines, respectively, after treatment with catalytic amount of PhjP. [Pg.411]


See other pages where 2- -2,5-alkadienoic acid 2-alkyn is mentioned: [Pg.2023]    [Pg.2023]    [Pg.2023]    [Pg.2024]    [Pg.2023]    [Pg.2023]    [Pg.2023]    [Pg.2023]    [Pg.2023]    [Pg.2023]    [Pg.2448]    [Pg.1064]    [Pg.2335]   
See also in sourсe #XX -- [ Pg.420 ]




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