Hirata Goki, Shimada Taisei, Nishikata Takashi
Graduate School of Science and Engineering, Yamaguchi University, Ube, Yamaguchi 755-8611, Japan.
Org Lett. 2020 Nov 20;22(22):8952-8956. doi: 10.1021/acs.orglett.0c03359. Epub 2020 Nov 4.
A light-driven atom-transfer radical substitution (ATRS) and carboesterification reaction of alkenes with alkyl halides has been developed using PTH as the organo-photoredox catalyst. Two types of products were obtained, depending on the additive and solvent used during the reaction. Primary, secondary, and tertiary alkyl halides reacted to give the ATRS products. This protocol has several advantages: it requires mild reaction conditions and a low catalyst loading and exhibits a broad substrate scope and good functional group tolerance. Mechanistic studies indicate that alkyl radicals might be generated as the key intermediates via photocatalysis, providing a new direction for ATRS reactions.
以PTH作为有机光氧化还原催化剂,实现了光驱动的烯烃与卤代烃的原子转移自由基取代(ATRS)和碳酯化反应。根据反应过程中使用的添加剂和溶剂不同,可得到两种类型的产物。伯、仲和叔卤代烃反应生成ATRS产物。该方法具有几个优点:反应条件温和,催化剂负载量低,底物范围广,官能团耐受性好。机理研究表明,烷基自由基可能是通过光催化生成的关键中间体,为ATRS反应提供了新的方向。