Direct enantioselective aldol reactions catalyzed by calix[4]arene-based L-proline derivatives in the water
dc.contributor.author | Eymur, Serkan | |
dc.contributor.author | Akceylan, Ezgi | |
dc.contributor.author | Sahin, Ozlem | |
dc.contributor.author | Uyanik, Arzu | |
dc.contributor.author | Yilmaz, Mustafa | |
dc.date.accessioned | 2020-03-26T18:50:06Z | |
dc.date.available | 2020-03-26T18:50:06Z | |
dc.date.issued | 2014 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | Two novel p-tert-butylcalix[4]arene-based chiral organocatalysts derived from L-proline have been developed to catalyze direct aldol reactions between cyclohexanone and aromatic aldehydes in water. Under the optimal conditions, high yields (up to 95%), enantioselectivities (up to 90%), and moderate diastereoselectivities (up to 65:35) were obtained. Considering the catalytic inefficiency of sole proline for the aldol reaction in water, these results clearly display the enormous effect of the hydrophobic part of calix[4]arene of compound A. (C) 2014 Elsevier Ltd. All rights reserved. | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TBAG-112T349]; Scientific Research Projects Foundation of Selcuk University (SUBAP)Selcuk University [14401006] | en_US |
dc.description.sponsorship | The authors gratefully acknowledge the Scientific and Technological Research Council of Turkey (TUBITAK-Grant Number TBAG-112T349), and Scientific Research Projects Foundation of Selcuk University (SUBAP-Grant Number 14401006). | en_US |
dc.identifier.doi | 10.1016/j.tet.2014.05.034 | en_US |
dc.identifier.endpage | 4477 | en_US |
dc.identifier.issn | 0040-4020 | en_US |
dc.identifier.issue | 30 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 4471 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1016/j.tet.2014.05.034 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/30746 | |
dc.identifier.volume | 70 | en_US |
dc.identifier.wos | WOS:000337868500003 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | en_US |
dc.relation.ispartof | TETRAHEDRON | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.subject | Calix[4]arene | en_US |
dc.subject | Organocatalysis | en_US |
dc.subject | Aldol | en_US |
dc.subject | Water | en_US |
dc.title | Direct enantioselective aldol reactions catalyzed by calix[4]arene-based L-proline derivatives in the water | en_US |
dc.type | Article | en_US |