Nickel(II) Bromide Catalyzed Multicomponent Cyclization to Access 4‐Substituted 2‐Iminothiazolines

IF 2.7 3区 化学 Q2 CHEMISTRY, ORGANIC
Vu H. Luu, Khoa H. D. Nguyen, Kien Q. Truong, Han B. Tran, Hoang V. M. Trinh, Thuy T. Ca, Tung T. Nguyen
{"title":"Nickel(II) Bromide Catalyzed Multicomponent Cyclization to Access 4‐Substituted 2‐Iminothiazolines","authors":"Vu H. Luu, Khoa H. D. Nguyen, Kien Q. Truong, Han B. Tran, Hoang V. M. Trinh, Thuy T. Ca, Tung T. Nguyen","doi":"10.1002/ejoc.202500830","DOIUrl":null,"url":null,"abstract":"A method is reported which allows for a three‐component cyclization of sulfoxonium ylides, aryl isothiocyanates, and amines to yield 2‐iminothiazolines. The method overcomes the limitation from the scope‐of‐substrate perspective. Success relies on the use of nickel(II) bromide, presumably acting as a Lewis acid catalyst. Investigation of substrate scopes reveals the compatibility of an array of useful functionalities.","PeriodicalId":167,"journal":{"name":"European Journal of Organic Chemistry","volume":"37 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/ejoc.202500830","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

A method is reported which allows for a three‐component cyclization of sulfoxonium ylides, aryl isothiocyanates, and amines to yield 2‐iminothiazolines. The method overcomes the limitation from the scope‐of‐substrate perspective. Success relies on the use of nickel(II) bromide, presumably acting as a Lewis acid catalyst. Investigation of substrate scopes reveals the compatibility of an array of useful functionalities.
镍(II)溴化催化多组分环化制备4 -取代的2 -亚氨基噻唑类化合物
报道了一种方法,该方法允许三组分环化亚砜酰化,芳基异硫氰酸酯和胺,以产生2 -亚氨基噻唑。该方法克服了从衬底范围角度的限制。成功依赖于溴化镍的使用,可能作为路易斯酸催化剂。对衬底作用域的研究揭示了一系列有用功能的兼容性。
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
CiteScore
5.40
自引率
3.60%
发文量
752
审稿时长
1 months
期刊介绍: The European Journal of Organic Chemistry (2019 ISI Impact Factor 2.889) publishes Full Papers, Communications, and Minireviews from the entire spectrum of synthetic organic, bioorganic and physical-organic chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. The following journals have been merged to form two leading journals, the European Journal of Organic Chemistry and the European Journal of Inorganic Chemistry: Liebigs Annalen Bulletin des Sociétés Chimiques Belges Bulletin de la Société Chimique de France Gazzetta Chimica Italiana Recueil des Travaux Chimiques des Pays-Bas Anales de Química Chimika Chronika Revista Portuguesa de Química ACH—Models in Chemistry Polish Journal of 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:604180095
Book学术官方微信