Bakhtiary Alireza, Poor Heravi Mohammad Reza, Hassanpour Akbar, Amini Issa, Vessally Esmail
Department of Chemistry, University of Alberta Edmonton Alberta T6G 2G2 Canada.
Department of Chemistry, Payame Noor University P.O. Box 19395-3697 Tehran Iran
RSC Adv. 2020 Dec 23;11(1):470-483. doi: 10.1039/d0ra08074h. eCollection 2020 Dec 21.
Due to the wide importance of β-phosphorylated ketones as key building-blocks in the fabrication of various pharmaceutically active organophosphorus compounds, finding new and truly efficient methods for their preparation from simple, low-cost and ubiquitous feedstock materials within a single click is an interesting subject in organic synthesis. Recently, oxyfunctionalization of carbon-carbon multiple bonds has arisen as a straightforward and versatile tool for the synthesis of complex organic molecules from the simple and easily accessible alkenes/alkynes a single operation. In this context, oxyphosphorylation of alkenes/alkynes with P(O)-H compounds has attracted considerable attention as a unique procedure for the construction of β-phosphorylated ketones. In this review, we outline the recent advances and developments in this fast-growing research field with particular emphasis on the mechanistic aspects of reaction.
由于β-磷酸化酮作为各种具有药学活性的有机磷化合物制备中的关键构建单元具有广泛的重要性,因此在有机合成中,找到从简单、低成本且普遍存在的原料材料一键式制备它们的新的且真正有效的方法是一个有趣的课题。最近,碳-碳多重键的氧官能化已成为一种直接且通用的工具,可通过单一操作从简单且易于获得的烯烃/炔烃合成复杂有机分子。在此背景下,烯烃/炔烃与P(O)-H化合物的氧膦酰化作为构建β-磷酸化酮的独特方法已引起了相当大的关注。在本综述中,我们概述了这一快速发展的研究领域的最新进展,特别强调了反应的机理方面。