Xiaojian Chen , Jun Zhang , Yang Gao, Qian Chen, Yanping Huo, Xianwei Li
{"title":"藤原-森谷反应：挑战与新机遇","authors":"Xiaojian Chen , Jun Zhang , Yang Gao, Qian Chen, Yanping Huo, Xianwei Li","doi":"10.1016/j.tchem.2025.100130","DOIUrl":null,"url":null,"abstract":"<div><div>Fujiwara-Moritani reaction has proven to be robust for the efficient construction of polyfunctionalized olefins and cyclic skeletons. Recent advances toward greener systems, compatibility with strongly coordinating heterocycle substrates and sterically hindered internal olefins, and achieving asymmetric catalysis have collectively opened new frontiers for Fujiwara-Moritani reaction.2009 Elsevier Ltd. All rights reserved.</div></div>","PeriodicalId":74918,"journal":{"name":"Tetrahedron chem","volume":"14 ","pages":"Article 100130"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fujiwara-Moritani reaction: challenges and new opportunities\",\"authors\":\"Xiaojian Chen , Jun Zhang , Yang Gao, Qian Chen, Yanping Huo, Xianwei Li\",\"doi\":\"10.1016/j.tchem.2025.100130\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Fujiwara-Moritani reaction has proven to be robust for the efficient construction of polyfunctionalized olefins and cyclic skeletons. Recent advances toward greener systems, compatibility with strongly coordinating heterocycle substrates and sterically hindered internal olefins, and achieving asymmetric catalysis have collectively opened new frontiers for Fujiwara-Moritani reaction.2009 Elsevier Ltd. All rights reserved.</div></div>\",\"PeriodicalId\":74918,\"journal\":{\"name\":\"Tetrahedron chem\",\"volume\":\"14 \",\"pages\":\"Article 100130\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron chem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666951X25000129\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666951X25000129","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fujiwara-Moritani reaction: challenges and new opportunities
Fujiwara-Moritani reaction has proven to be robust for the efficient construction of polyfunctionalized olefins and cyclic skeletons. Recent advances toward greener systems, compatibility with strongly coordinating heterocycle substrates and sterically hindered internal olefins, and achieving asymmetric catalysis have collectively opened new frontiers for Fujiwara-Moritani reaction.2009 Elsevier Ltd. All rights reserved.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
