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Enantioselective Sequential‐Flow Synthesis of Baclofen Precursor via Asymmetric 1,4‐Addition and Chemoselective Hydrogenation on Platinum/Carbon/Calcium Phosphate Composites

Haruro Ishitani, Yuichi Furiya, Shū Kobayashi

2020Chemistry - An Asian Journal26 citationsDOI

Abstract

Continuous-flow synthesis of baclofen precursor (2) was achieved using achiral and chiral heterogeneous catalysts in high yield with high enantioselectivity. The key steps are chiral calcium-catalyzed asymmetric 1,4-addition of a malonate to a nitroalkene and chemoselective reduction of a nitro compound to the corresponding amino compound by using molecular hydrogen. A dimethylpolysilane (DMPS)-modified platinum catalyst supported on activated carbon (AC) and calcium phosphate (CP) has been developed that has remarkable activity for the selective hydrogenation of nitro compounds.

Topics & Concepts

Enantioselective synthesisCatalysisPlatinumMalonateChemistryYield (engineering)Carbon fibersNitroOrganic chemistryCombinatorial chemistryMaterials scienceComposite materialComposite numberAlkylInnovative Microfluidic and Catalytic Techniques InnovationAsymmetric Hydrogenation and CatalysisChemical Synthesis and Analysis
Enantioselective Sequential‐Flow Synthesis of Baclofen Precursor via Asymmetric 1,4‐Addition and Chemoselective Hydrogenation on Platinum/Carbon/Calcium Phosphate Composites | Litcius