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Heavy atom carbene analogues

Among the heavy atom carbene analogues, the chemistry of silylenes has been covered by two reviews. A first one describes the reactivity of 2,2,5,5-tetrakis(trimethylsilyl) silacyclopentane-l,l-diyl with a focus on mechanistic discussions. The nature of the reactions (radical with haloalkanes, concerted insertion with OH, SiH and SiCl)... [Pg.178]

The fert-butyl group is known as one of the most effective kinetic protectors and many reactive molecules have been stabilized and even isolated by using this group. For example, the divalent center of silylenes and germylenes, the heavy atom analogues of carbenes, have been shown to be blocked by tcrt-butyl groups. [Pg.441]


See other pages where Heavy atom carbene analogues is mentioned: [Pg.199]    [Pg.227]    [Pg.177]    [Pg.209]    [Pg.171]    [Pg.203]    [Pg.199]    [Pg.227]    [Pg.177]    [Pg.209]    [Pg.171]    [Pg.203]    [Pg.279]    [Pg.115]   
See also in sourсe #XX -- [ Pg.178 ]




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Carbenes heavy-atom analogues

Carbenes heavy-atom carbene analogues

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