Williams Catherine M, Johnson Jeffrey B, Rovis Tomislav
Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, USA.
J Am Chem Soc. 2008 Nov 12;130(45):14936-7. doi: 10.1021/ja8062925. Epub 2008 Oct 17.
A nickel-catalyzed reductive carboxylation of styrenes using CO2 has been developed. The reaction proceeds under mild conditions using diethylzinc as the reductant. Preliminary data suggests the mechanism involves two discrete nickel-mediated catalytic cycles, the first involving a catalyzed hydrozincation of the alkene followed by a second, slower nickel-catalyzed carboxylation of the in situ formed organozinc reagent. Importantly, the catalyst system is very robust and will fixate CO2 in good yield even if exposed to only an equimolar amount introduced into the headspace above the reaction.
已开发出一种使用二氧化碳对苯乙烯进行镍催化的还原羧基化反应。该反应在温和条件下进行,使用二乙基锌作为还原剂。初步数据表明其机理涉及两个独立的镍介导催化循环,第一个循环涉及烯烃的催化氢锌化反应,随后是第二个较慢的镍催化原位形成的有机锌试剂的羧基化反应。重要的是,该催化剂体系非常稳定,即使仅暴露于引入反应上方顶空的等摩尔量的二氧化碳中,也能以良好的产率固定二氧化碳。