{"title":"手性Brønsted酸催化双芳基苯酚与酰胺的分子间氢苯氧基化反应","authors":"Yu Yu , Min Chen","doi":"10.1039/d5ob00503e","DOIUrl":null,"url":null,"abstract":"<div><div>Herein we disclose the first catalytic asymmetric intermolecular hydrophenoxylation of ynamides with biaryl phenols under chiral Brønsted acid catalysis, providing axially chiral phenols. This enantioselective reaction proceeds through a sequential desymmetrizaiton/kinetic resolution process, which features mild reaction conditions and represents a rare paradigm of an organocatalytic asymmetric intermolecular reaction of ynamides.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 22","pages":"Pages 5318-5322"},"PeriodicalIF":2.7000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chiral Brønsted acid-catalyzed intermolecular hydrophenoxylation of ynamides with biaryl phenols via sequential desymmetrization/kinetic resolution†\",\"authors\":\"Yu Yu , Min Chen\",\"doi\":\"10.1039/d5ob00503e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein we disclose the first catalytic asymmetric intermolecular hydrophenoxylation of ynamides with biaryl phenols under chiral Brønsted acid catalysis, providing axially chiral phenols. This enantioselective reaction proceeds through a sequential desymmetrizaiton/kinetic resolution process, which features mild reaction conditions and represents a rare paradigm of an organocatalytic asymmetric intermolecular reaction of ynamides.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 22\",\"pages\":\"Pages 5318-5322\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025003866\",\"RegionNum\":3,\"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 & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025003866","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Chiral Brønsted acid-catalyzed intermolecular hydrophenoxylation of ynamides with biaryl phenols via sequential desymmetrization/kinetic resolution†
Herein we disclose the first catalytic asymmetric intermolecular hydrophenoxylation of ynamides with biaryl phenols under chiral Brønsted acid catalysis, providing axially chiral phenols. This enantioselective reaction proceeds through a sequential desymmetrizaiton/kinetic resolution process, which features mild reaction conditions and represents a rare paradigm of an organocatalytic asymmetric intermolecular reaction of ynamides.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.