Jie Zhou , Zhizheng Chen , Mengna Nie , Wenhao Li , Wen-Yan Tong , Haonan Wei , Hang Yan , Qianwen Gao , Shuanglin Qu , Xi Wang
{"title":"镍催化烯系肟酯与二硫代磺酸的对映选择性还原亚氨基二磺化反应","authors":"Jie Zhou , Zhizheng Chen , Mengna Nie , Wenhao Li , Wen-Yan Tong , Haonan Wei , Hang Yan , Qianwen Gao , Shuanglin Qu , Xi Wang","doi":"10.1039/d5cc01654a","DOIUrl":null,"url":null,"abstract":"<div><div>A novel nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate is presented in this study. This reaction exhibits exceptional regio- and enantioselectivity, showing broad substrate compatibility. Gram-scale synthesis of chiral pyrroline disulfide and versatile subsequent conversions highlight the synthetic utility of this scaffold.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 40","pages":"Pages 7329-7332"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate†\",\"authors\":\"Jie Zhou , Zhizheng Chen , Mengna Nie , Wenhao Li , Wen-Yan Tong , Haonan Wei , Hang Yan , Qianwen Gao , Shuanglin Qu , Xi Wang\",\"doi\":\"10.1039/d5cc01654a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A novel nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate is presented in this study. This reaction exhibits exceptional regio- and enantioselectivity, showing broad substrate compatibility. Gram-scale synthesis of chiral pyrroline disulfide and versatile subsequent conversions highlight the synthetic utility of this scaffold.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 40\",\"pages\":\"Pages 7329-7332\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-04-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525008055\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734525008055","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate†
A novel nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate is presented in this study. This reaction exhibits exceptional regio- and enantioselectivity, showing broad substrate compatibility. Gram-scale synthesis of chiral pyrroline disulfide and versatile subsequent conversions highlight the synthetic utility of this scaffold.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.