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Peroxometallacycle intermediate

Pd(H) fcrf-butyl peroxidic complexes of the general formula [RCOOPdOOferf-Bu]4 are very efficient reagents for the selective stoichiometric oxidation of terminal alkenes in anhydrous nonbasic organic solvents at ambient temperature.518 They also catalyze the ketonization by tert-BuOOH. Internal olefins are not reactive at all. A peroxometallacycle intermediate (see discussion below) was suggested. [Pg.473]

Deuterium labeling experiments indicate that ketone formation involves a peroxometallacycle intermediate, but epoxidation occurs via a different path [174]. [Pg.142]

Peroxometallacycles are also regarded as active intermediates in olefin epoxidation by diperoxomolybdenum(VI) and related reagents (cf. section 3.1.1. ). [Pg.139]


See other pages where Peroxometallacycle intermediate is mentioned: [Pg.1075]    [Pg.1075]    [Pg.51]    [Pg.1075]    [Pg.1075]    [Pg.51]    [Pg.131]    [Pg.141]    [Pg.170]   
See also in sourсe #XX -- [ Pg.457 , Pg.473 ]




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