Photo‐triggered Intramolecular Radical Tandem Regioselective Alkylation/Cyclization of 1,6‐Dienes with Redox‐Active Esters Enabled by an EDA Complex.

Autor: Sun, Bin, Ling, Lan, Zhuang, Xiaohui, Yang, Lulu, Yin, Jieli, Jin, Can
Předmět:
Zdroj: Chinese Journal of Chemistry; Jan2023, Vol. 41 Issue 1, p37-42, 6p
Abstrakt: Comprehensive Summary: A photocatalyst‐ and metal‐free radical tandem alkylation/cyclization between 1,6‐dienes and redox‐active esters has been developed, affording a series of N‐aryl pyrrolidine‐2‐ones in moderate to good yields. The transformation is driven by the formation of an electron‐donor‐acceptor (EDA) complex and a subsequent single electron transfer (SET) process. This photocatalyst‐free protocol features excellent regioselectivity, mild conditions and broad substrate scope, providing a facile access to 3‐alkyl‐3,4‐dimethyl‐1‐phenylpyrrolidin‐2‐one. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index