Show simple item record

dc.contributor.authorLevandowski, Brian J
dc.contributor.authorRaines, Ronald T
dc.date.accessioned2022-03-16T17:55:13Z
dc.date.available2022-03-16T17:55:13Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/141236
dc.description.abstractCyclopentadiene is one of the most reactive dienes in normal electron-demand Diels-Alder reactions. The high reactivities and yields of cyclopentadiene cycloadditions make them ideal as click reactions. In this review, we discuss the history of the cyclopentadiene cycloaddition as well as applications of cyclopentadiene click reactions. Our emphasis is on experimental and theoretical studies on the reactivity and stability of cyclopentadiene and cyclopentadiene derivatives.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACS.CHEMREV.0C01055en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleClick Chemistry with Cyclopentadieneen_US
dc.typeArticleen_US
dc.identifier.citationLevandowski, Brian J and Raines, Ronald T. 2021. "Click Chemistry with Cyclopentadiene." Chemical Reviews, 121 (12).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.relation.journalChemical Reviewsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-03-16T17:51:48Z
dspace.orderedauthorsLevandowski, BJ; Raines, RTen_US
dspace.date.submission2022-03-16T17:51:50Z
mit.journal.volume121en_US
mit.journal.issue12en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record