Iterative One-Carbon Homologation of Unmodified Carboxylic Acids

被引:1
作者
Wheatley, Emilie [1 ,2 ]
Melnychenko, Heorhii [1 ,2 ]
Silvi, Mattia [1 ,2 ]
机构
[1] Univ Nottingham, GSK Carbon Neutral Labs Sustainable Chem, Nottingham NG7 2TU, England
[2] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国科研创新办公室; 英国工程与自然科学研究理事会;
关键词
ALPHA-AMINO-ACIDS; ARNDT-EISTERT REACTION; PHOTOREDOX CATALYSIS; VISIBLE-LIGHT; BETA-PEPTIDES; CONJUGATE ADDITIONS; ESTER HOMOLOGATION; RADICAL CHEMISTRY; ACYL DERIVATIVES; FORMAL SYNTHESIS;
D O I
10.1021/jacs.4c13630
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:34285 / 34291
页数:7
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