Silver-Catalyzed Tandem Cyclization of Sulfur Ylides with Terminal Alkynes: Direct Synthesis of Vinylcyclopropanes

IF 4.6 1区 化学 Q1 CHEMISTRY, ORGANIC
Yue Gong, Xue-Cen Xu, Yu-Xuan Meng, Yu-Long Zhao
{"title":"Silver-Catalyzed Tandem Cyclization of Sulfur Ylides with Terminal Alkynes: Direct Synthesis of Vinylcyclopropanes","authors":"Yue Gong, Xue-Cen Xu, Yu-Xuan Meng, Yu-Long Zhao","doi":"10.1039/d5qo00012b","DOIUrl":null,"url":null,"abstract":"A novel silver-catalyzed tandem cyclization reaction of electron-deficient terminal alkynes with two molecules of sulfur ylides has been developed. The reaction provides a simple and highly efficient strategy for the synthesis of diversely functionalized vinylcyclopropanes from easily available acyclic starting materials with good to high diastereoselectivities in a single step. Mechanistic studies indicate a sequential reaction mechanism that involves methyl migration, nucleophilic addition, cyclization, electrocyclic ring-opening, and cyclopropanation. Further applications, including synthesis of vinylcyclopropanes bearing dihydroxyl groups, 3-oxabicyclo[3.1.0]hexanes and biphenyls, demonstrated the immense potential of the tandem cyclization.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":"51 1","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qo00012b","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

A novel silver-catalyzed tandem cyclization reaction of electron-deficient terminal alkynes with two molecules of sulfur ylides has been developed. The reaction provides a simple and highly efficient strategy for the synthesis of diversely functionalized vinylcyclopropanes from easily available acyclic starting materials with good to high diastereoselectivities in a single step. Mechanistic studies indicate a sequential reaction mechanism that involves methyl migration, nucleophilic addition, cyclization, electrocyclic ring-opening, and cyclopropanation. Further applications, including synthesis of vinylcyclopropanes bearing dihydroxyl groups, 3-oxabicyclo[3.1.0]hexanes and biphenyls, demonstrated the immense potential of the tandem cyclization.
我们开发出了一种新型的银催化串联环化反应,可使缺电子的末端炔烃与两分子硫酰化物发生反应。该反应提供了一种简单、高效的策略,可从易于获得的无环起始材料中合成多种官能化乙烯基环丙烷,且一步即可获得良好甚至较高的非对映选择性。机理研究表明,其反应机理包括甲基迁移、亲核加成、环化、电环开环和环丙烷化。进一步的应用,包括合成带有二羟基的乙烯基环丙烷、3-氧杂双环[3.1.0]己烷和联苯,证明了串联环化反应的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信