Shinichi Itsuno, Katsuhiro Watanabe, Takahiro Koizumi, Koichi Ito
{"title":"Asymmetric Diels-Alder reaction of cyclopentadiene with methacrolein using polymer-supported chiral catalysts","authors":"Shinichi Itsuno, Katsuhiro Watanabe, Takahiro Koizumi, Koichi Ito","doi":"10.1016/0923-1137(94)00087-L","DOIUrl":null,"url":null,"abstract":"<div><p>Polymer-supported chiral Lewis acids were prepared from bromoboranes and crosslinked polymers having chiral amino alcohol or diol moieties. These polymers were used as chiral catalysts for Diels-Alder reactions of cyclopentadiene with methacrolein to give optically active cycloadduct in high chemical yield with high <em>exo</em> selectivity. Optical yield up to 54% ee was obtained by the use of polymeric chiral catalyst derived from (<em>S</em>)-proline. The potential of this type of approach in asymmetric synthesis is discussed.</p></div>","PeriodicalId":20864,"journal":{"name":"Reactive Polymers","volume":"24 3","pages":"Pages 219-227"},"PeriodicalIF":0.0000,"publicationDate":"1995-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0923-1137(94)00087-L","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive Polymers","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/092311379400087L","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 24
Abstract
Polymer-supported chiral Lewis acids were prepared from bromoboranes and crosslinked polymers having chiral amino alcohol or diol moieties. These polymers were used as chiral catalysts for Diels-Alder reactions of cyclopentadiene with methacrolein to give optically active cycloadduct in high chemical yield with high exo selectivity. Optical yield up to 54% ee was obtained by the use of polymeric chiral catalyst derived from (S)-proline. The potential of this type of approach in asymmetric synthesis is discussed.