Access to Fully Substituted Furans via Boryl Radical Catalyzed Cycloisomerization of Cyclopropenyl Ketones

IF 2.8 4区 化学 Q1 CHEMISTRY, ORGANIC
Xingran Yang , Jiahang Li , Prof. Dr. Jinbo Zhao
{"title":"Access to Fully Substituted Furans via Boryl Radical Catalyzed Cycloisomerization of Cyclopropenyl Ketones","authors":"Xingran Yang ,&nbsp;Jiahang Li ,&nbsp;Prof. Dr. Jinbo Zhao","doi":"10.1002/ajoc.202500126","DOIUrl":null,"url":null,"abstract":"<div><div>We report the boryl radical catalyzed cycloisomerization of cyclopropenyl ketones to fully‐substituted furans, a type of highly important pharmacophore and synthetic intermediate. The reaction features neutral conditions, high yields, and toleration of variation at all possible positions of the substrate, making it an indispensable route for this type of important scaffold. Preliminary downstream transformation also revealed the synthetic potential of these furans in accessing other types of furans or more complex 3D scaffolds.</div></div>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"14 7","pages":"Article e202500126"},"PeriodicalIF":2.8000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2193580725002314","RegionNum":4,"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

We report the boryl radical catalyzed cycloisomerization of cyclopropenyl ketones to fully‐substituted furans, a type of highly important pharmacophore and synthetic intermediate. The reaction features neutral conditions, high yields, and toleration of variation at all possible positions of the substrate, making it an indispensable route for this type of important scaffold. Preliminary downstream transformation also revealed the synthetic potential of these furans in accessing other types of furans or more complex 3D scaffolds.
硼基自由基催化环丙烯酮环异构化制备全取代呋喃
我们报道了硼基自由基催化环丙烯酮环异构化成完全取代呋喃,这是一种非常重要的药效团和合成中间体。该反应条件中性,产率高,并且在底物的所有可能位置都能耐受变化,使其成为这种重要支架不可缺少的途径。初步的下游转化也揭示了这些呋喃在获取其他类型呋喃或更复杂的3D支架方面的合成潜力。
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
CiteScore
4.70
自引率
3.70%
发文量
372
期刊介绍: Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC) The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.
×
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