铂催化的 1,8-二氨基萘保护二硼酸(B2(dan)2)对炔烃的二化反应

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
Shinichi Saito*, Yuya Koizumi, Yuki Ito, Taiga Yasuda and Yusuke Yoshigoe, 
{"title":"铂催化的 1,8-二氨基萘保护二硼酸(B2(dan)2)对炔烃的二化反应","authors":"Shinichi Saito*,&nbsp;Yuya Koizumi,&nbsp;Yuki Ito,&nbsp;Taiga Yasuda and Yusuke Yoshigoe,&nbsp;","doi":"10.1021/acs.joc.4c0193910.1021/acs.joc.4c01939","DOIUrl":null,"url":null,"abstract":"<p >The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.</p>","PeriodicalId":57,"journal":{"name":"The Journal of Organic Chemistry","volume":"89 22","pages":"16947–16951 16947–16951"},"PeriodicalIF":3.3000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.joc.4c01939","citationCount":"0","resultStr":"{\"title\":\"Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)\",\"authors\":\"Shinichi Saito*,&nbsp;Yuya Koizumi,&nbsp;Yuki Ito,&nbsp;Taiga Yasuda and Yusuke Yoshigoe,&nbsp;\",\"doi\":\"10.1021/acs.joc.4c0193910.1021/acs.joc.4c01939\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"The Journal of Organic Chemistry\",\"volume\":\"89 22\",\"pages\":\"16947–16951 16947–16951\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.joc.4c01939\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.4c01939\",\"RegionNum\":2,\"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":"The Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.4c01939","RegionNum":2,"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

摘要

在铂催化剂存在下,1,8-二氨基萘保护二硼酸(B2(dan)2)对炔烃的二加成反应进展顺利,分离出的 1,2-二硼酸烯的产率高达 94%。使用适当的溶剂和配体对反应的进展至关重要。对 1,2-二芳基烯的衍生化进行了简要研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)

The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B2(dan)2) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
The Journal of Organic Chemistry
The Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: The Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
×
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:481959085
Book学术官方微信