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在[bmim][Br]中铋介导的醛的烯丙基化反应:机理研究

Bi-mediated allylation of aldehydes in [bmim][Br]: a mechanistic investigation.

作者信息

Koli Mrunesh, Chatterjee Sucheta, Chattopadhyay Subrata, Goswami Dibakar

机构信息

Bio-Organic Division, Bhabha Atomic Research Centre, Mumbai - 400 085, India.

Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai - 400 094, India.

出版信息

Beilstein J Org Chem. 2018 Aug 22;14:2198-2203. doi: 10.3762/bjoc.14.193. eCollection 2018.

Abstract

The inexpensive room temperature ionic liquid (RTIL), [bmim][Br] has been found to be a superior medium for the Bi-mediated Barbier-type allylation of aldehydes compared to other conventional solvents. It plays the dual role of a solvent and a metal activator enabling higher yields of the products in a shorter reaction time using stoichiometric/near-stoichiometric amounts of reagents. Plausibly, [bmim][Br] activates Bi metal by a charge transfer mechanism. The H VT-NMR studies suggested that both the allylating species, allylbismuth dibromide and diallylbismuth bromide, are generated in situ.

摘要

已发现廉价的室温离子液体(RTIL)[bmim][Br]与其他传统溶剂相比,是用于铋介导的醛的巴比耶型烯丙基化反应的优良介质。它起到溶剂和金属活化剂的双重作用,能够在使用化学计量/接近化学计量的试剂时,在更短的反应时间内获得更高产率的产物。合理推测,[bmim][Br]通过电荷转移机制活化铋金属。高分辨核磁共振(H VT-NMR)研究表明,烯丙基化物种二溴烯丙基铋和溴化二烯丙基铋均是原位生成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70aa/6122318/3a3a4ae49a4b/Beilstein_J_Org_Chem-14-2198-g004.jpg

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