{"title":"铜(I)催化二芳基膦硫化物与醛胺的不对称加成反应。","authors":"Dong-Liang Xie , Hu Tian , Liang Yin","doi":"10.1039/d5ob00682a","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we report a copper(<span>i</span>)-catalyzed enantioselective addition of diarylphosphine sulfides to <em>N</em>-thiophosphinoyl aldimines. The reaction offers some advantages, such as mild conditions, an easy protocol, and high enantioselectivity. Control experiments indicate that the “soft–soft” interactions between the copper(<span>i</span>) catalyst and the sulfur atoms in both diarylphosphine sulfides and <em>N</em>-thiophosphinoyl aldimines facilitate the addition.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 25","pages":"Pages 6106-6110"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Copper(i)-catalyzed asymmetric addition of diarylphosphine sulfides to aldimines†\",\"authors\":\"Dong-Liang Xie , Hu Tian , Liang Yin\",\"doi\":\"10.1039/d5ob00682a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, we report a copper(<span>i</span>)-catalyzed enantioselective addition of diarylphosphine sulfides to <em>N</em>-thiophosphinoyl aldimines. The reaction offers some advantages, such as mild conditions, an easy protocol, and high enantioselectivity. Control experiments indicate that the “soft–soft” interactions between the copper(<span>i</span>) catalyst and the sulfur atoms in both diarylphosphine sulfides and <em>N</em>-thiophosphinoyl aldimines facilitate the addition.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 25\",\"pages\":\"Pages 6106-6110\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-04-01\",\"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/S1477052025004574\",\"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/S1477052025004574","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Copper(i)-catalyzed asymmetric addition of diarylphosphine sulfides to aldimines†
Herein, we report a copper(i)-catalyzed enantioselective addition of diarylphosphine sulfides to N-thiophosphinoyl aldimines. The reaction offers some advantages, such as mild conditions, an easy protocol, and high enantioselectivity. Control experiments indicate that the “soft–soft” interactions between the copper(i) catalyst and the sulfur atoms in both diarylphosphine sulfides and N-thiophosphinoyl aldimines facilitate the addition.
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.