dc.contributor.author | Levandowski, Brian J | |
dc.contributor.author | Raines, Ronald T | |
dc.date.accessioned | 2022-03-16T17:55:13Z | |
dc.date.available | 2022-03-16T17:55:13Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/141236 | |
dc.description.abstract | Cyclopentadiene 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.iso | en | |
dc.publisher | American Chemical Society (ACS) | en_US |
dc.relation.isversionof | 10.1021/ACS.CHEMREV.0C01055 | en_US |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
dc.source | PMC | en_US |
dc.title | Click Chemistry with Cyclopentadiene | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Levandowski, Brian J and Raines, Ronald T. 2021. "Click Chemistry with Cyclopentadiene." Chemical Reviews, 121 (12). | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | |
dc.relation.journal | Chemical Reviews | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2022-03-16T17:51:48Z | |
dspace.orderedauthors | Levandowski, BJ; Raines, RT | en_US |
dspace.date.submission | 2022-03-16T17:51:50Z | |
mit.journal.volume | 121 | en_US |
mit.journal.issue | 12 | en_US |
mit.license | OPEN_ACCESS_POLICY | |
mit.metadata.status | Authority Work and Publication Information Needed | en_US |