Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives
dc.contributor.author | Genc, Hayriye Nevin | |
dc.date.accessioned | 2024-02-23T14:16:46Z | |
dc.date.available | 2024-02-23T14:16:46Z | |
dc.date.issued | 2019 | |
dc.department | NEÜ | en_US |
dc.description.abstract | A highly enantioselective Michael addition reaction of anthrone with nitroalkenes by chiral tetraoxacalix[2]arene[2]triazine catalysts was investigated as a novel topic. The stereoselective conversion progressed smoothly by employing 10 mol% of the catalyst and afforded the corresponding Michael adducts with acceptable to high enantioselectivities (up to 97% ee) and very high yields (up to 96%). | en_US |
dc.identifier.doi | 10.1039/c9ra03029h | |
dc.identifier.endpage | 21069 | en_US |
dc.identifier.issn | 2046-2069 | |
dc.identifier.issue | 36 | en_US |
dc.identifier.pmid | 35515554 | en_US |
dc.identifier.scopus | 2-s2.0-85068548987 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 21063 | en_US |
dc.identifier.uri | https://doi.org/10.1039/c9ra03029h | |
dc.identifier.uri | https://hdl.handle.net/20.500.12452/12788 | |
dc.identifier.volume | 9 | en_US |
dc.identifier.wos | WOS:000474306500064 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Soc Chemistry | en_US |
dc.relation.ispartof | Rsc Advances | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | [Keyword Not Available] | en_US |
dc.title | Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives | en_US |
dc.type | Article | en_US |