Two‐Phase Electrosynthesis of Dihydroxycoumestans: Discovery of a New Scaffold for Topoisomerase I poison DOI

Yue‐Xi Chen,

Shanchao Wu, Xiang Shen

и другие.

Chemistry - A European Journal, Год журнала: 2024, Номер 30(39)

Опубликована: Май 13, 2024

Coumestan represents a biologically relevant structural motif distributed in number of natural products, and the rapid construction related derivatives as well characterization targets would accelerate lead compound discovery medicinal chemistry. In this work, general scalable approach to 8,9-dihydroxycoumestans via two-electrode constant current electrolysis was developed. The application two-phase (aqueous/organic) system plays crucial role for success, protecting sensitive o-benzoquinone intermediates from over-oxidation. Based on structurally diverse primary SAR study coumestan scaffold completed, 3 r exhibited potent antiproliferative activities robust topoisomerase I (Top1) inhibitory activity. Further mechanism studies demonstrates that novel Top1 poison, which might open an avenue development Top1-targeted antitumor agent.

Язык: Английский

Electrochemical chemoselective thiocarbamylation of late-stage Tyr-containing drugs and peptides DOI

Wan‐Jie Wei,

Xinyu Wang, Haitao Tang

и другие.

Science China Chemistry, Год журнала: 2024, Номер 67(10), С. 3382 - 3388

Опубликована: Авг. 2, 2024

Язык: Английский

Процитировано

23

Paired Electrolysis-Enabled Arylation of Quinoxalin-2(1H)-ones DOI

Jia-Cheng Hou,

Jun Jiang,

Yan-Cui Wen

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(9), С. 6117 - 6125

Опубликована: Апрель 24, 2024

The first paired electrolysis-enabled arylation of quinoxalin-2(1H)-ones was achieved using cyanoarenes as the reagents. A variety 3-arylquinoxalin-2(1H)-ones with various important functional groups were obtained in moderate to good yields under metal- and chemical oxidant-free conditions. With a pair reductive oxidative processes occurring among substrates reaction intermediates, power consumption can be dramatically reduced.

Язык: Английский

Процитировано

21

Electrochemical difunctionalization of alkenes and alkynes for the synthesis of organochalcogens involving C–S/Se bond formation DOI
Jianchao Liu, Jie‐Ping Wan, Yunyun Liu

и другие.

Organic Chemistry Frontiers, Год журнала: 2023, Номер 11(2), С. 597 - 630

Опубликована: Ноя. 23, 2023

This review highlights the recent progress in electrochemical difunctionalization of alkenes and alkynes involving C–S/Se bond formation to access organochalcogen frameworks.

Язык: Английский

Процитировано

30

An electrocatalytic mono-functionalization of alkenes towards alkenyl selenium sulfonates DOI

Zhiheng Zhao,

Hongyan Yan,

Lijun Gu

и другие.

Chemical Communications, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

In this study, a straightforward and environmentally benign electrochemical mono-functionalization of alkenes has been established for the synthesis alkenyl selenium sulfonates using elemental as source.

Язык: Английский

Процитировано

1

Regioselective electrochemical cascade C–H sulfonylation–bromination of indolizines to access difunctionalized indolizines DOI
Wenxuan Jiang, Xiang Liu, Chuanying Zhu

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(8), С. 2306 - 2312

Опубликована: Янв. 1, 2024

Regioselective electrochemical C–H sulfonylation–bromination between indolizines, sodium sulfinates, and KBr has been established in an undivided cell, which serves as both the brominating agent electrolyte.

Язык: Английский

Процитировано

7

Electrochemical epoxidation of alkene with high faradaic efficiencies using water as an oxygen source DOI
Hao Bin Wu,

Yousen Xu,

Pengyu Guo

и другие.

Green Chemistry, Год журнала: 2024, Номер 26(5), С. 2922 - 2927

Опубликована: Янв. 1, 2024

An efficient electrochemical epoxidation of alkenes catalyzed by (TMP)MnCl with water as the oxygen source is disclosed. The reaction achieved impressive faradaic efficiencies (up to 89%) for a broad range substrates.

Язык: Английский

Процитировано

6

Advances in photochemical/electrochemical synthesis of heterocyclic compounds from carbon dioxide DOI
Yuyang Xie, Ying‐Ming Pan

Green Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

This paper reviews progress in the photochemical/electrochemical construction of heterocyclic compounds using CO 2 , differentiating between various reaction types and elucidating their underlying mechanisms as well potential applications.

Язык: Английский

Процитировано

5

Controllable Construction of Vinyl Sulfones and β‐Keto Selenosulfones via Selective Oxidative Sulfonylation of Alkenes DOI
Xiang Liu, Yuan Zhang, Yi Zheng

и другие.

Chinese Journal of Chemistry, Год журнала: 2024, Номер 42(12), С. 1367 - 1372

Опубликована: Фев. 23, 2024

Comprehensive Summary The selective oxidative sulfonylation of alkenes with selenium sulfonate depended on the reaction conditions. electrochemical C—H proceeded smoothly to afford ( E )‐vinyl sulfones good selectivity in an undivided cell without external oxidant. While aerobic trifunctionalization occurred presence KI air, which provides β ‐keto selenosulfones via formation C—O, C—S, and C—Se bonds one‐pot. Following control experiments, a plausible mechanism is proposed rationalize experimental results.

Язык: Английский

Процитировано

4

Recent Advances in Electrochemical-Promoted Unactivated C(sp3)—H Functionalization DOI

Ruilin Gao,

Li‐Rong Wen, Wei‐Si Guo

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(3), С. 892 - 892

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

4

Electrochemically mediated synthesis of trifluoromethylallenes DOI
Jialan Zhang,

Jin-Xiu Xiong,

Lu‐Qi Fei

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(12), С. 3485 - 3490

Опубликована: Янв. 1, 2024

Herein, we report electrochemically mediated trifluoromethylallene synthesis via the rearrangement of trifluoromethyl-containing 1,3-enynes under action silicon or boron radicals, with good selectivity and without external oxidants.

Язык: Английский

Процитировано

4