Pregled bibliografske jedinice broj: 886044
Rationalization of Enantioselectivity Change in Rhodium-catalyzed Hydrogenation Reaction Assessed by DFT Calculations
Rationalization of Enantioselectivity Change in Rhodium-catalyzed Hydrogenation Reaction Assessed by DFT Calculations // 20th European Symposium on Organic Chemistry (ESOC 2017)
Köln, Njemačka, 2017. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 886044 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Rationalization of Enantioselectivity Change in Rhodium-catalyzed Hydrogenation Reaction Assessed by DFT Calculations
Autori
Glasovac, Zoran ; Kokan, Zoran ; Kirin Srećko I.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
20th European Symposium on Organic Chemistry (ESOC 2017)
Mjesto i datum
Köln, Njemačka, 02.07.2017. - 06.07.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
enantioselectivity reversal, DFT method
Sažetak
In continuation of our efforts to optimize "backdoor induction" of chirality in rhodium catalyzed hydrogenation of methyl α-acetamidoacrylate (substrate), influence of rigidity of the used ligands was investigated. We have recently demonstrated enantioselectivity control simply by switching from two monodentate to one bidentate ligand without change in point chirality at the stereogenic centers nor helicity of the formed complexes. To find the origin of these results, we investigated mechanism of the reaction and differences in the reaction pathways that lead to either of two possible enantiomeric products. In this regard, we relied on the findings of Gridnev and Imamoto who identified a substrate double bond approach toward Rh atom as the process along which enantioselection takes place. Also, this process most likely occur after oxidative addition of hydrogen. Assuming similar mechanism, we modeled possible reaction pathways along which enantioselection takes place employing wB97XD DFT method. Four possible structures of each supramolecular and enediyne tethered semicoordinated complexes were used as the initial points. Experimentally observed enantioselectivity reversal was interpreted in terms of the reaction energetics and geometrical changes along the Rh-"ene" bond formation paths. Ligand change induces strong destabilization of otherwise the most probable S-path which becomes the least probable one. R-paths are also destabilized but to lesser extent.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-1461 - Minimalni umjetni enzimi: Proširenje primjene posredne indukcije na nove supstrate i nove asimetrične reakcije (MArtEn) (Kirin, Srećko, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
