亲核细胞
化学
结合
电泳剂
试剂
区域选择性
组合化学
加成反应
烯烃纤维
立体选择性
分子
级联
选择性
计算化学
有机化学
催化作用
色谱法
数学分析
数学
作者
Paola Vitale,Vito Capriati,Saverio Florio,Filippo Maria Perna,Antonio Salomone
标识
DOI:10.2174/1385272820666161021161644
摘要
Conjugate addition reactions of organometallic compounds to electron-poor olefins is a versatile synthetic methodology for the formation of new carbon–carbon bonds. However, a careful control of the regioselectivity of the process is needed because of the presence of two electrophilic sites in the activated olefin. This issue is often overcome by employing "soft" nucleophiles such as organocopper and organozinc reagents, because of their high selectivity towards the 1,4-addition. In contrast, organolithium compounds, which are "hard" nucleophiles, generally give access to 1,2-adducts, 1,4-conjugate addition being sometimes observed according to the nature of nucleophiles and/or electrophiles, or to the presence of additives. In this Minireview, we have described some peculiar examples to get an outline of the recent acquisitions in the field of the conjugate additions of functionalized organolithiums to electron-poor olefins. Particular attention is paid to the synthesis of complex structures starting from simple substrates by means of cascade reactions promoted by conjugate addition reactions with organolithiums. Keywords: Organolithiums, conjugate addition, alkenes, heterocycles, stereoselectivity, cascade reactions.
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