• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

电化学促进的合成不对称硫代磺酸酯的三组分反应。

Electrochemical promoted three-component reaction to unsymmetric thiosulfonates.

作者信息

Lin Hong-Min, Ren Sai-Yan, Cui Fei-Hu, Pan Ying-Ming, Tang Hai-Tao

机构信息

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Collaborative Innovation Center for Guangxi Ethnic Medicine, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, People's Republic of China.

出版信息

Chem Commun (Camb). 2024 Sep 16;60(75):10394-10397. doi: 10.1039/d4cc03570d.

DOI:10.1039/d4cc03570d
PMID:39224062
Abstract

Compounds comprising S-S bonds serve as significant pharmacological scaffolds in medicinal chemistry and natural products. We have devised an efficient electrochemical method for the construction of asymmetric disulfide bonds, leading to the synthesis of unsymmetric thiosulfonates. Compared with existing synthesis methods, our work not only avoids the use of metals and oxidants, but also realizes the operation of a one-pot three-component method, which makes this strategy extremely attractive.

摘要

包含S-S键的化合物在药物化学和天然产物中是重要的药理支架。我们设计了一种高效的电化学方法来构建不对称二硫键,从而合成不对称硫代磺酸酯。与现有的合成方法相比,我们的工作不仅避免了使用金属和氧化剂,还实现了一锅三组分法的操作,这使得该策略极具吸引力。

相似文献

1
Electrochemical promoted three-component reaction to unsymmetric thiosulfonates.电化学促进的合成不对称硫代磺酸酯的三组分反应。
Chem Commun (Camb). 2024 Sep 16;60(75):10394-10397. doi: 10.1039/d4cc03570d.
2
Photo-induced decarboxylative C-S bond formation to access sterically hindered unsymmetric S-alkyl thiosulfonates and SS-alkyl thiosulfonates.通过光诱导脱羧形成碳-硫键以合成空间位阻不对称的S-烷基硫代磺酸盐和S,S-二烷基硫代磺酸盐。
Nat Commun. 2024 Aug 25;15(1):7313. doi: 10.1038/s41467-024-51334-5.
3
Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted -Thiocarbamates: Easy Access to the S-SO Bond.从N-取代硫代氨基甲酸盐出发合成不对称硫代磺酸酯:轻松构建S-SO键
J Org Chem. 2022 Sep 2;87(17):11656-11668. doi: 10.1021/acs.joc.2c01301. Epub 2022 Aug 12.
4
Efficient unsymmetric disulfide formation by molecular-scale tailoring of ortho-polyquinone-based polymer photocatalyst.通过对基于邻位聚醌的聚合物光催化剂进行分子尺度剪裁实现高效不对称二硫键形成
J Colloid Interface Sci. 2025 Jan 15;678(Pt A):1022-1030. doi: 10.1016/j.jcis.2024.08.224. Epub 2024 Aug 30.
5
Nickel-catalyzed selective disulfide formation by reductive cross-coupling of thiosulfonates.镍催化硫代磺酸盐还原交叉偶联选择性形成二硫化物。
Chem Sci. 2024 Aug 30;15(37):15474-9. doi: 10.1039/d4sc02969k.
6
Hypervalent iodine(iii)-promoted rapid cascade reaction for the synthesis of unsymmetric azo compounds.高价碘(III)促进的快速串联反应合成不对称偶氮化合物。
Org Biomol Chem. 2021 Apr 14;19(14):3119-3123. doi: 10.1039/d1ob00219h. Epub 2021 Mar 23.
7
Visible-Light-Driven Unsymmetric -Difunctionalization of Vinyl Azides with Thiosulfonates or Selenosulfonates.可见光驱动的叠氮乙烯与硫代磺酸盐或硒代磺酸盐的不对称双官能化反应
Org Lett. 2024 Mar 1;26(8):1683-1687. doi: 10.1021/acs.orglett.4c00183. Epub 2024 Feb 16.
8
Copper-Catalyzed Oxidative Carbon-Carbon and/or Carbon-Heteroatom Bond Formation with O or Internal Oxidants.铜催化的与氧或内氧化剂的碳-碳和/或碳-杂原子键的氧化形成反应。
Acc Chem Res. 2018 May 15;51(5):1092-1105. doi: 10.1021/acs.accounts.7b00611. Epub 2018 Apr 12.
9
Disproportionate Coupling Reaction of Sodium Sulfinates Mediated by BF·OEt: An Approach to Symmetrical/Unsymmetrical Thiosulfonates.BF·OEt 介导的亚磺酸钠的不均衡偶联反应:一种合成对称/不对称硫代磺酸盐的方法。
Org Lett. 2018 Aug 17;20(16):4754-4758. doi: 10.1021/acs.orglett.8b01808. Epub 2018 Aug 1.
10
Coupling of 1-Chloro-,-diisopropylphosphanamine-Based Reagents with Alcohols and Thiosulfonates: A Precise Construction of O-P(O)-S Bonds.基于1-氯-,-二异丙基膦胺的试剂与醇和硫代磺酸盐的偶联:O-P(O)-S键的精确构建
Org Lett. 2022 Jul 29;24(29):5324-5328. doi: 10.1021/acs.orglett.2c01947. Epub 2022 Jul 14.