Herein,a rapid alkenylation of quinoxalin-2(1H)-ones enabled by a combination of Mannich-type reaction and solar photocatalysis is demonstrated.A wide range of functional groups are compatible,affording the correspond...Herein,a rapid alkenylation of quinoxalin-2(1H)-ones enabled by a combination of Mannich-type reaction and solar photocatalysis is demonstrated.A wide range of functional groups are compatible,affording the corresponding products in moderate-to-good yields.Control experiments illustrate that the in situ generated^(1)O_(2)plays a central role in this reaction.This green and efficient strategy provides a practical solution for the synthesis of potentially bioactive compounds that containing a 3,4-dihydroquinoxalin-2(1H)-one structure.展开更多
Herein, an efficient molecular oxygen-mediated method for the selective hydroxyalkylation and alkylation of quinoxalin-2(1 H)-ones with alkylboronic acids under transition-metal free conditions has been developed. Thi...Herein, an efficient molecular oxygen-mediated method for the selective hydroxyalkylation and alkylation of quinoxalin-2(1 H)-ones with alkylboronic acids under transition-metal free conditions has been developed. This strategy demonstrates a broad scope of quinoxalin-2(1 H)-ones and alkylboronic acids, giving3-hydroxyalkylquinoxalin-2(1 H)-ones and 3-alkylquinoxalin-2(1 H)-ones in moderate-to-good yield. Control experiments reveal that a radical pathway is involved.展开更多
基金the Natural Science Foundation of Zhejiang Province(No.LY21B060009)the National Natural Science Foundation of China(No.21871071)for financial support.
文摘Herein,a rapid alkenylation of quinoxalin-2(1H)-ones enabled by a combination of Mannich-type reaction and solar photocatalysis is demonstrated.A wide range of functional groups are compatible,affording the corresponding products in moderate-to-good yields.Control experiments illustrate that the in situ generated^(1)O_(2)plays a central role in this reaction.This green and efficient strategy provides a practical solution for the synthesis of potentially bioactive compounds that containing a 3,4-dihydroquinoxalin-2(1H)-one structure.
基金Natural Science Foundation of Zhejiang Province(No. LY21B060009) for financial support。
文摘Herein, an efficient molecular oxygen-mediated method for the selective hydroxyalkylation and alkylation of quinoxalin-2(1 H)-ones with alkylboronic acids under transition-metal free conditions has been developed. This strategy demonstrates a broad scope of quinoxalin-2(1 H)-ones and alkylboronic acids, giving3-hydroxyalkylquinoxalin-2(1 H)-ones and 3-alkylquinoxalin-2(1 H)-ones in moderate-to-good yield. Control experiments reveal that a radical pathway is involved.