2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with N-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways.

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
The Journal of Organic Chemistry Pub Date : 2024-11-15 Epub Date: 2024-11-05 DOI:10.1021/acs.joc.4c01877
Dennis Sulwey, Julia B DiSapio, José A Gascón, Amy R Howell
{"title":"2-Halomethyleneoxetanes from 2-Methyleneoxetanes by Reaction with <i>N</i>-Halosuccinimides: Reactant Influences on Stereochemical Outcomes and Reaction Pathways.","authors":"Dennis Sulwey, Julia B DiSapio, José A Gascón, Amy R Howell","doi":"10.1021/acs.joc.4c01877","DOIUrl":null,"url":null,"abstract":"<p><p>The first general synthesis of 2-halomethyleneoxetanes, realized by the reaction of 2-methyleneoxetanes with <i>N</i>-halosuccinimides (NXS), is reported. The relative diastereoselectivities of the transformations were dependent on the halogen of NXS, while alternative reaction outcomes were influenced by substituents on the oxetane. Quantum mechanical calculations and molecular dynamics simulations exploring the basis of the observed diastereoselectivities are described. These highly strained heterocycles underwent standard cross-coupling reactions, demonstrating their utility as synthetic intermediates.</p>","PeriodicalId":57,"journal":{"name":"The Journal of Organic Chemistry","volume":" ","pages":"16571-16585"},"PeriodicalIF":3.3000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Organic Chemistry","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.joc.4c01877","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

The first general synthesis of 2-halomethyleneoxetanes, realized by the reaction of 2-methyleneoxetanes with N-halosuccinimides (NXS), is reported. The relative diastereoselectivities of the transformations were dependent on the halogen of NXS, while alternative reaction outcomes were influenced by substituents on the oxetane. Quantum mechanical calculations and molecular dynamics simulations exploring the basis of the observed diastereoselectivities are described. These highly strained heterocycles underwent standard cross-coupling reactions, demonstrating their utility as synthetic intermediates.

Abstract Image

通过与 N-卤代丁二酰亚胺反应制备 2-亚甲基氧杂环丁烷:反应物对立体化学结果和反应途径的影响。
本研究首次报道了通过 2-亚甲基氧杂环丁烷与 N-卤代丁二酰亚胺(NXS)反应合成 2-亚甲基氧杂环丁烷的一般方法。转化的相对非对映选择性取决于 NXS 的卤素,而其他反应结果则受到氧杂环丁烷上取代基的影响。本文介绍了探索所观察到的非对映选择性基础的量子力学计算和分子动力学模拟。这些高度紧张的杂环进行了标准的交叉耦合反应,证明了它们作为合成中间体的实用性。
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
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