The first application of C2-symmetric ferrocenyl phosphinite ligands for rhodium-catalyzed asymmetric transfer hydrogenation of various ketones
dc.contributor.author | Ak, Bunyamin | |
dc.contributor.author | Aydemir, Murat | |
dc.contributor.author | Durap, Feyyaz | |
dc.contributor.author | Meric, Nermin | |
dc.contributor.author | Baysal, Akin | |
dc.date.accessioned | 2024-04-24T16:14:52Z | |
dc.date.available | 2024-04-24T16:14:52Z | |
dc.date.issued | 2015 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Homogeneous catalysis has been responsible for many major recent developments in synthetic organic chemistry. The combined use of organometallic and coordination chemistry has produced a number of new and powerful synthetic methods for important classes of compounds in general and for optically active substances in particular. For this aim, a new class of chiral modular C-2-symmetric ferrocenyl phosphinite ligands has been prepared in good yields by using the inexpensive 1,1'-ferrocenedicarboxyaldehyde and various ferrocene based-amino alcohols as starting materials, and applied in the rhodium(I)-catalyzed asymmetric transfer hydrogenation (ATH) of aromatic ketones to give corresponding secondary alcohols with excellent enantioselectivities and reactivities using isoPrOH as the hydrogen source (up to 99% conversion and 99% ee). The substituents on the backbone of the ligands are found to exhibit a remarkable effect on both the activity and % ee. The structures of these ligands and their complexes have been elucidated by a combination of multinuclear NMR spectroscopy, IR spectroscopy and elemental analysis. (C) 2015 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | Tubitak [111T419] | en_US |
dc.description.sponsorship | Financial support from Tubitak (Project number: 111T419) is gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1016/j.ica.2015.09.003 | |
dc.identifier.endpage | 51 | en_US |
dc.identifier.issn | 0020-1693 | |
dc.identifier.issn | 1873-3255 | |
dc.identifier.scopus | 2-s2.0-84942626748 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 42 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ica.2015.09.003 | |
dc.identifier.uri | https://hdl.handle.net/11468/15462 | |
dc.identifier.volume | 438 | en_US |
dc.identifier.wos | WOS:000363867500008 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Sa | en_US |
dc.relation.ispartof | Inorganica Chimica Acta | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Asymmetric Catalysis | en_US |
dc.subject | C-2-Symmetric Ferrocenyl Phosphinite | en_US |
dc.subject | Asymmetric Transfer Hydrogenation | en_US |
dc.subject | Aromatic Ketones | en_US |
dc.subject | Rhodium(I) | en_US |
dc.title | The first application of C2-symmetric ferrocenyl phosphinite ligands for rhodium-catalyzed asymmetric transfer hydrogenation of various ketones | en_US |
dc.title | The first application of C2-symmetric ferrocenyl phosphinite ligands for rhodium-catalyzed asymmetric transfer hydrogenation of various ketones | |
dc.type | Article | en_US |