Syntheses, structures, and reactivities of borylcopper and -zinc compounds:: 1,4-silaboration of an α,β-unsaturated ketone to form a γ-siloxyallylborane
Syntheses, structures, and reactivities of borylcopper and -zinc compounds:: 1,4-silaboration of an α,β-unsaturated ketone to form a γ-siloxyallylborane
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DOI:
10.1002/anie.200801728
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发表时间:
2008-01-01
影响因子:
16.6
通讯作者:
Nozaki, Kyoko
中科院分区:
文献类型:
--
作者:
Kajiwara, Takashi;Terabayashi, Tomomi;Nozaki, Kyoko
Carbanions are one of the most important reagents in synthetic organic chemistry.[1] They act as a carbon nucleophile to form a carbon–carbon bond as a consequence of the highly polarized carbon–metal bonds (CdÀÀMd+). The properties of polar carbon–metal bonds in a carbanionic species depend on the metallic counterpart, such as lithium, magnesium, copper, and zinc. The first two organometallic compounds directly attack the carbonyl group of a, b-unsaturated ketones, whereas the latter two [2] react by 1, 4-addition (conjugate addition).[3]