Transition metal-catalyzed transformations of 2-formylarylboronic acids

IF 2.7 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-08-28 Epub Date: 2024-08-14 DOI:10.1039/d4ob01024h
Fatemeh Doraghi , Amir Mohammad Taherkhani , Tolou Hosseinifar , Parviz Rashidi Ranjbar , Bagher Larijani , Mohammad Mahdavi
{"title":"Transition metal-catalyzed transformations of 2-formylarylboronic acids","authors":"Fatemeh Doraghi ,&nbsp;Amir Mohammad Taherkhani ,&nbsp;Tolou Hosseinifar ,&nbsp;Parviz Rashidi Ranjbar ,&nbsp;Bagher Larijani ,&nbsp;Mohammad Mahdavi","doi":"10.1039/d4ob01024h","DOIUrl":null,"url":null,"abstract":"<div><p>2-Formylarylboronic acids are easily available precursors in organic chemistry. Different types of transition metal catalysts, such as Pd(0), Pd(<span>ii</span>), Rh(<span>i</span>), Ir(<span>i</span>), Ni(<span>ii</span>), Cu(<span>i</span>), Cu(<span>ii</span>), and Co(<span>ii</span>), can efficiently catalyze coupling reactions of 2-formylarylboronic acids with other organic reactants. In this review, we describe the synthesis of a diverse range of carbocyclic and heterocyclic compounds, as well as acyclic compounds, <em>via</em> transition metal-catalyzed reactions of 2-formylarylboronic acids over the past two decades.</p></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"22 34","pages":"Pages 6905-6921"},"PeriodicalIF":2.7000,"publicationDate":"2024-08-28","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/S1477052024007043","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

2-Formylarylboronic acids are easily available precursors in organic chemistry. Different types of transition metal catalysts, such as Pd(0), Pd(ii), Rh(i), Ir(i), Ni(ii), Cu(i), Cu(ii), and Co(ii), can efficiently catalyze coupling reactions of 2-formylarylboronic acids with other organic reactants. In this review, we describe the synthesis of a diverse range of carbocyclic and heterocyclic compounds, as well as acyclic compounds, via transition metal-catalyzed reactions of 2-formylarylboronic acids over the past two decades.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
过渡金属催化的 2-甲酰基芳基硼酸转化。
2-甲酰基硼酸是有机化学中很容易获得的前体。不同类型的过渡金属催化剂,如 Pd(0)、Pd(II)、Rh(I)、Ir(I)、Ni(II)、Cu(I)、Cu(II) 和 Co(II),可以有效催化 2-甲酰基硼酸与其他有机反应物的偶联反应。在本综述中,我们介绍了过去二十年中通过过渡金属催化 2-甲酰基芳基硼酸反应合成各种碳环和杂环化合物以及无环化合物的情况。
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 去求助
来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
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.
期刊最新文献
Copper-catalyzed radical 1,2-oxysulfoximination of β,γ-unsaturated oximes for the synthesis of sulfoximine-substituted isoxazolines. RhIII-catalyzed C-H heteroarylation and C-N cleavage: direct access to C2-heteroarylated (NH)-indoles. Recent advances in the deuteration of indoles. Stereodivergent (3 + 2)-cycloaddition of donor-acceptor cyclopropanes and citral imines catalyzed by Yb(NTf2)3/PyBOX. PyfSeTs as a novel and photosensitive reagent for green light-induced arene C-H selenenylation: a versatile strategy for the synthesis of aryl selenides.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1