An article Direct Asymmetric Hydrogenation and Dynamic Kinetic Resolution of Aryl Ketones Catalyzed by an Iridium-NHC Exhibiting High Enantio- and Diastereoselectivity WOS:000510786100001 published article about N-HETEROCYCLIC CARBENES; STEREODIRECTING LIGANDS; STEREOSELECTIVE HYDROGENATION; RHODIUM COMPLEXES; HYDROSILYLATION; ALKENES; BEARING in [Swamy, Chinna Ayya P.; Varenikov, Andrii; de Ruiter, Graham] Technion Israel Inst Technol, Schulich Fac Chem, IL-3200008 Haifa, Israel in 2020.0, Cited 67.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6
A chiral iridium carbene-oxazoline catalyst is reported that is able to directly and efficiently hydrogenate a wide variety of ketones in excellent yields and good enantioselectivity (up to 93 % ee). Moreover, when using racemic alpha-substituted ketones, excellent diastereoselectivities were obtained (dr 99:1) by dynamic kinetic resolution of the in situ formed enolate. Overall, the herein described hydrogenation occurs under ambient conditions using low hydrogen pressures, providing a direct and atom efficient method towards chiral secondary alcohols.
Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Swamy, PCA; Varenikov, A; de Ruiter, G or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem