Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
Chem Asian J. 2020 Aug 17;15(16):2428-2436. doi: 10.1002/asia.202000606. Epub 2020 Jul 13.
Potential widespread applications of organoarsenic chemistry have been limited by the inherent lack of safe and effective As-C bond formation reactions. Several alternative reagents and methods have been developed in the last few decades to address the hazards and drawbacks associated with traditional arsenic synthetic strategies. Herein, this minireview summarizes the advances made in nucleophilic, electrophilic, radical and metal-mediated As(III)-C bond formations while specifically highlighting the behavior of arsenic synthons with various well-established reagents (eg. Grignard reagents, organolithium compounds, organometallic reagents, radical initiators and Lewis/Brønsted bases). Avenues for asymmetric synthesis are also discussed, as are recent advances in organoarsenic chemistry suggesting that arsines exhibit novel reactivities independent from that of other relatively more well explored Group V cogeners.
有机砷化学的潜在广泛应用受到安全有效形成 As-C 键反应的固有缺乏的限制。在过去几十年中,已经开发出几种替代试剂和方法来解决与传统砷合成策略相关的危险和缺点。本文综述了亲核、亲电、自由基和金属介导的 As(III)-C 键形成方面的进展,同时特别强调了各种成熟试剂(如格氏试剂、有机锂化合物、有机金属试剂、自由基引发剂和路易斯/布朗斯台德碱)中砷合成子的行为。还讨论了不对称合成的途径,以及有机砷化学的最新进展表明胂表现出与其他相对更深入研究的 V 族同系物不同的新颖反应性。