Enantioselective Aldol Reaction between Isatins and Ketones, Catalyzed by Chiral Norephedrine-Derived ?-Amino Alcohols with a Thiophene Moiety
dc.contributor.author | Aydin, A. E. | |
dc.date.accessioned | 2024-09-18T20:16:50Z | |
dc.date.available | 2024-09-18T20:16:50Z | |
dc.date.issued | 2022 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Chiral norephedrine-based beta-amino alcohol bearing a substituted thiophene ring were applied as catalysts for the enantioselective aldol reaction of isatins with ketones. Using enantiomeric chiral amino alco-hols, the desired aldol products were obtained in high yields and excellent enantioselectivities (up to 95% ee) under optimized conditions. | en_US |
dc.identifier.doi | 10.1134/S1070428022060100 | |
dc.identifier.endpage | 829 | en_US |
dc.identifier.issn | 1070-4280 | |
dc.identifier.issn | 1608-3393 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.scopus | 2-s2.0-85135604307 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 820 | en_US |
dc.identifier.uri | https://doi.org/10.1134/S1070428022060100 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/9769 | |
dc.identifier.volume | 58 | en_US |
dc.identifier.wos | WOS:000837686700010 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Maik Nauka/Interperiodica/Springer | en_US |
dc.relation.ispartof | Russian Journal of Organic Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | enantioselective reaction | en_US |
dc.subject | aldol reaction | en_US |
dc.subject | chiral amino alcohols | en_US |
dc.subject | isatin | en_US |
dc.title | Enantioselective Aldol Reaction between Isatins and Ketones, Catalyzed by Chiral Norephedrine-Derived ?-Amino Alcohols with a Thiophene Moiety | en_US |
dc.type | Article | en_US |
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