{"title":"串联磷二硫基化/烯丙醇与P4S10和醇重排构建烯丙基磷二硫代酸酯","authors":"Jian Huang, Yingjie Wang, Yufen Lv, Xiaohui Zhao, Zu-Li Wang, Wei Wei* and Dong Yi*, ","doi":"10.1021/acs.joc.5c0076110.1021/acs.joc.5c00761","DOIUrl":null,"url":null,"abstract":"<p >An additive-free approach has been developed for the synthesis of allylic phosphorodithioates through tandem phosphorodithiolation/rearrangement of allylic alcohols with P<sub>4</sub>S<sub>10</sub> and alcohols. The reaction proceeds under mild conditions and provides a practical protocol to prepare a series of allylic phosphorodithioates in moderate to good yields.</p>","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"90 23","pages":"7849–7856 7849–7856"},"PeriodicalIF":3.6000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tandem Phosphorodithiolation/Rearrangement of Allylic Alcohols with P4S10 and Alcohols to Construct Allylic Phosphorodithioates\",\"authors\":\"Jian Huang, Yingjie Wang, Yufen Lv, Xiaohui Zhao, Zu-Li Wang, Wei Wei* and Dong Yi*, \",\"doi\":\"10.1021/acs.joc.5c0076110.1021/acs.joc.5c00761\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >An additive-free approach has been developed for the synthesis of allylic phosphorodithioates through tandem phosphorodithiolation/rearrangement of allylic alcohols with P<sub>4</sub>S<sub>10</sub> and alcohols. The reaction proceeds under mild conditions and provides a practical protocol to prepare a series of allylic phosphorodithioates in moderate to good yields.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"90 23\",\"pages\":\"7849–7856 7849–7856\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.5c00761\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.5c00761","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Tandem Phosphorodithiolation/Rearrangement of Allylic Alcohols with P4S10 and Alcohols to Construct Allylic Phosphorodithioates
An additive-free approach has been developed for the synthesis of allylic phosphorodithioates through tandem phosphorodithiolation/rearrangement of allylic alcohols with P4S10 and alcohols. The reaction proceeds under mild conditions and provides a practical protocol to prepare a series of allylic phosphorodithioates in moderate to good yields.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.