Unusual selectivity in the ring-opening of γ-valerolactone oxide by amines
| dc.contributor.author | Mazloomi, Zahra | en |
| dc.contributor.author | Kallmeier, Fabian | en |
| dc.contributor.author | Kirchhecker, Sarah | en |
| dc.contributor.author | Stadler, Bernhard M. | en |
| dc.contributor.author | Pandey, Swechchha | en |
| dc.contributor.author | Schünemann, Claas | en |
| dc.contributor.author | Spannenberg, Anke | en |
| dc.contributor.author | Hering-Junghans, Christian | en |
| dc.contributor.author | Tin, Sergey | en |
| dc.contributor.author | de Vries, Johannes G. | en |
| dc.contributor.author | Baráth, Eszter | en |
| dc.date.accessioned | 2026-07-03T23:40:31Z | |
| dc.date.available | 2026-07-03T23:40:31Z | |
| dc.date.issued | 2023-06-13 | en |
| dc.description.abstract | Primary and secondary amines selectively react with the lactone moiety of γ-valerolactone oxide (GVLO). Several primary amines afforded the resulting epoxyamides with an intact epoxy group. In some cases addition of two equivalents of amine resulted in additional epoxide opening to give α,γ-dihydroxy-β-amino-amides. The selective lactone-opening in GVLO was further corroborated by DFT-studies. | en |
| dc.description.status | Peer-reviewed | en |
| dc.format.extent | 4 | en |
| dc.identifier.issn | 1359-7345 | en |
| dc.identifier.other | PubMed:37337749 | en |
| dc.identifier.other | ORCID:/0000-0001-7073-2766/work/219173118 | en |
| dc.identifier.scopus | 85163975548 | en |
| dc.identifier.uri | https://hdl.handle.net/1885/733812786 | |
| dc.language.iso | en | en |
| dc.rights | Publisher Copyright: © 2023 The Royal Society of Chemistry. | en |
| dc.source | Chemical Communications | en |
| dc.title | Unusual selectivity in the ring-opening of γ-valerolactone oxide by amines | en |
| dc.type | Journal article | en |
| dspace.entity.type | Publication | en |
| local.bibliographicCitation.lastpage | 8447 | en |
| local.bibliographicCitation.startpage | 8444 | en |
| local.contributor.affiliation | Mazloomi, Zahra; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Kallmeier, Fabian; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Kirchhecker, Sarah; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Stadler, Bernhard M.; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Pandey, Swechchha; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Schünemann, Claas; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Spannenberg, Anke; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Hering-Junghans, Christian; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Tin, Sergey; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | de Vries, Johannes G.; Leibniz Institute for Catalysis | en |
| local.contributor.affiliation | Baráth, Eszter; Leibniz Institute for Catalysis | en |
| local.identifier.citationvolume | 59 | en |
| local.identifier.doi | 10.1039/d3cc01957h | en |
| local.identifier.pure | 884aa06a-df30-4805-9e73-89e8139cafe4 | en |
| local.identifier.url | https://www.scopus.com/pages/publications/85163975548 | en |
| local.type.status | Published | en |