Wheatley Emilie, Melnychenko Heorhii, Silvi Mattia
The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Nottingham NG7 2TU, United Kingdom.
School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom.
J Am Chem Soc. 2024 Dec 18;146(50):34285-34291. doi: 10.1021/jacs.4c13630. Epub 2024 Dec 10.
The one-carbon homologation of carboxylic acids is a valuable route to construct families of homologues, which play fundamental roles in chemistry and biology. However, known procedures are based on multistep sequences, use harsh conditions or are limited in scope. Thus, almost a century after the discovery of the original Arndt-Eistert homologation sequence, a general method to directly convert carboxylic acids into their corresponding homologues remains elusive. Exploiting the photoredox reactivity of nitroethylene, we disclose a practical visible-light-induced homologation of unmodified carboxylic acids. Iterations of the procedure reveal an exceptionally tunable strategy for the construction of inert carbon spacers, opening new opportunities in synthesis.
羧酸的一碳同系化是构建同系物家族的一条有价值的途径,这些同系物在化学和生物学中起着基础性作用。然而,已知的方法基于多步序列,使用苛刻的条件或范围有限。因此,在最初的阿恩特-艾斯特尔特同系化序列发现近一个世纪后,一种直接将羧酸转化为其相应同系物的通用方法仍然难以捉摸。利用硝基乙烯的光氧化还原反应活性,我们揭示了一种实用的可见光诱导的未修饰羧酸的同系化反应。该过程的迭代揭示了一种用于构建惰性碳间隔基的异常可调策略,为合成开辟了新的机会。