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Decarboxylative etherification

Can an alkyl aryl ether be prepared through a decarboxylative etherification process ... [Pg.84]

The material is prepared by etherification of 4-methylpyrocatechol with two equivalents of alkyl 2-bromoacetate, and subsequent Dieckmann condensation followed by hydrolysis and decarboxylation [195a]. [Pg.151]

Examples. Either or both microwave reactors have been useful for processes such as esterification, amidation, transesterification, rearrangement, acetalization, nucleophilic substitution, hydrolysis of esters and amides, isomerization, decarboxylation, oxidation, elimination, etherification, and formation of aminoreductones. Examples of such reactions have been tabulated (2,3). [Pg.275]

Scheme 11.7 Decarboxylative allylic etherifications illustrating the enhanced thermal stability of dbcot complexes. Scheme 11.7 Decarboxylative allylic etherifications illustrating the enhanced thermal stability of dbcot complexes.
Some of the typical reactions that take place during an alkyd resin preparation and curing are (1) esterification, (2) alcoholysis, (3) ester interchange or transesterification, (4) etherification, (5) free radical addition reactions, (6) Diels-Alder reactions, (7) decarboxylations, and (8) polymerization via free radical initiation during curing (air-drying alkyds). [Pg.162]

See other pages where Decarboxylative etherification is mentioned: [Pg.217]    [Pg.74]    [Pg.74]    [Pg.217]    [Pg.74]    [Pg.74]    [Pg.333]    [Pg.49]    [Pg.352]    [Pg.1421]    [Pg.112]    [Pg.176]    [Pg.342]    [Pg.244]    [Pg.323]    [Pg.332]    [Pg.494]    [Pg.323]   
See also in sourсe #XX -- [ Pg.74 , Pg.84 ]



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