钯催化的乙烯基烯烃在水†上的对映选择性酯化反应

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Junhua Li, Yaqian Min and Yian Shi
{"title":"钯催化的乙烯基烯烃在水†上的对映选择性酯化反应","authors":"Junhua Li, Yaqian Min and Yian Shi","doi":"10.1039/D4NJ02253J","DOIUrl":null,"url":null,"abstract":"<p >An efficient Pd-catalyzed asymmetric hydroesterification of vinyl arenes on water is reported. A variety of phenyl 2-arylpropanoates can be obtained in good yields with high b/l ratios and ee's with phenyl formate or CO as a carbonyl source. (<em>R</em>)-DTBM-SEGPHOS was found to be an effective ligand for the reaction under aqueous conditions. The hydrophobicity of the ligand appeared to be crucial to the hydroesterification reaction, which likely proceeded “on water”.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pd-catalyzed enantioselective hydroesterification of vinyl arenes on water†\",\"authors\":\"Junhua Li, Yaqian Min and Yian Shi\",\"doi\":\"10.1039/D4NJ02253J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >An efficient Pd-catalyzed asymmetric hydroesterification of vinyl arenes on water is reported. A variety of phenyl 2-arylpropanoates can be obtained in good yields with high b/l ratios and ee's with phenyl formate or CO as a carbonyl source. (<em>R</em>)-DTBM-SEGPHOS was found to be an effective ligand for the reaction under aqueous conditions. The hydrophobicity of the ligand appeared to be crucial to the hydroesterification reaction, which likely proceeded “on water”.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj02253j\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj02253j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本研究报道了在 Pd 催化下,乙烯基烯烃在水中的高效不对称酯化反应。以甲酸苯酯或 CO 为羰基源,可以获得多种 2-芳基丙酸苯酯,产率高,b/l 比和 ee 值高。研究发现,(R)-DTBM-SEGPHOS 是在水性条件下进行反应的有效配体。配体的疏水性似乎对可能在 "水上 "进行的酯化反应至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pd-catalyzed enantioselective hydroesterification of vinyl arenes on water†

An efficient Pd-catalyzed asymmetric hydroesterification of vinyl arenes on water is reported. A variety of phenyl 2-arylpropanoates can be obtained in good yields with high b/l ratios and ee's with phenyl formate or CO as a carbonyl source. (R)-DTBM-SEGPHOS was found to be an effective ligand for the reaction under aqueous conditions. The hydrophobicity of the ligand appeared to be crucial to the hydroesterification reaction, which likely proceeded “on water”.

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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in 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:481959085
Book学术官方微信