{"title":"环丙基烯丙醇开环亲核取代制备(E)-δ-乙烯基均烯丙醇/醚/吡唑","authors":"Yulu Zhang, Ying Shao, Jiangtao Sun, Shengbiao Tang","doi":"10.1039/d5qo00678c","DOIUrl":null,"url":null,"abstract":"A highly efficient Lewis acid-catalyzed ring-opening nucleophilic substitution of cyclopropyl allylic alcohols has been developed. The use of pyrazoles as nucleophiles, under catalysis with Yb(OTf)3, a series of (E)-δ-vinyl-homoallylic pyrazoles were obtained in moderate to good yields. When the use of water or alcohols as nucleophiles, under the catalyst of Ga(OTf)3, the desired (E)-δ-Vinyl-homoallylic alcohols/ethers were achieved. The cyclopropyl allylic alcohols have been successfully employed for the first time in ring-opening nucleophilic substitution reactions. This method features mild condition, good functional group tolerance.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":"138 1","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Access to (E)-δ-Vinyl-Homoallylic Alcohols/Ethers/Pyrazoles by Ring-opening Nucleophilic Substitution of cyclopropyl allylic alcohols\",\"authors\":\"Yulu Zhang, Ying Shao, Jiangtao Sun, Shengbiao Tang\",\"doi\":\"10.1039/d5qo00678c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A highly efficient Lewis acid-catalyzed ring-opening nucleophilic substitution of cyclopropyl allylic alcohols has been developed. The use of pyrazoles as nucleophiles, under catalysis with Yb(OTf)3, a series of (E)-δ-vinyl-homoallylic pyrazoles were obtained in moderate to good yields. When the use of water or alcohols as nucleophiles, under the catalyst of Ga(OTf)3, the desired (E)-δ-Vinyl-homoallylic alcohols/ethers were achieved. The cyclopropyl allylic alcohols have been successfully employed for the first time in ring-opening nucleophilic substitution reactions. This method features mild condition, good functional group tolerance.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\"138 1\",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-05-24\",\"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/d5qo00678c\",\"RegionNum\":1,\"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":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qo00678c","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Access to (E)-δ-Vinyl-Homoallylic Alcohols/Ethers/Pyrazoles by Ring-opening Nucleophilic Substitution of cyclopropyl allylic alcohols
A highly efficient Lewis acid-catalyzed ring-opening nucleophilic substitution of cyclopropyl allylic alcohols has been developed. The use of pyrazoles as nucleophiles, under catalysis with Yb(OTf)3, a series of (E)-δ-vinyl-homoallylic pyrazoles were obtained in moderate to good yields. When the use of water or alcohols as nucleophiles, under the catalyst of Ga(OTf)3, the desired (E)-δ-Vinyl-homoallylic alcohols/ethers were achieved. The cyclopropyl allylic alcohols have been successfully employed for the first time in ring-opening nucleophilic substitution reactions. This method features mild condition, good functional group tolerance.
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.