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Bromomethyl group, size

Carbonylative cycloaddition of allyl bromides and acetylenes in methanol in the presence of nickel tetracarbonyl results in the formation of cyclopentenones. For instance, 3-bromocyclopentene and methyl but-2-ynoate afford the diester 493, the halogen atom being replaced by the methoxycarbonyl group. Nickel tetracarbonyl also catalyses the reaction of l-(bromomethyl) cycloalkenes 494 of ring size 5-8 with methyl but-2-ynoate in methanol to yield the spiro-compounds 495 (equation 54). ... [Pg.344]


See other pages where Bromomethyl group, size is mentioned: [Pg.397]    [Pg.12]    [Pg.516]    [Pg.22]    [Pg.463]    [Pg.45]    [Pg.932]    [Pg.763]   
See also in sourсe #XX -- [ Pg.34 ]




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