{"title":"Relative Cycloaddition Rates of Alkyne-Equivalent Dienophiles","authors":"Tucker J. Hamilton, Christopher M. Beaudry","doi":"10.1021/acs.joc.4c03028","DOIUrl":null,"url":null,"abstract":"Alkyne-equivalent dienophiles are strategically important coupling partners in Diels–Alder reactions. They are particularly useful in cascade bond-forming processes that begin with cycloadditions. A systematic rate study for the cycloaddition of several alkyne and alkyne-equivalent dienophiles is presented, showing that the relative reaction rates of these dienophiles vary over multiple orders of magnitude.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"73 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.4c03028","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
Abstract
Alkyne-equivalent dienophiles are strategically important coupling partners in Diels–Alder reactions. They are particularly useful in cascade bond-forming processes that begin with cycloadditions. A systematic rate study for the cycloaddition of several alkyne and alkyne-equivalent dienophiles is presented, showing that the relative reaction rates of these dienophiles vary over multiple orders of magnitude.
期刊介绍:
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.