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Mn(<scp>i</scp>) phosphine-amino-phosphinites: a highly modular class of pincer complexes for enantioselective transfer hydrogenation of aryl-alkyl ketones

Harikrishnan Jayaprakash

2021Dalton Transactions22 citationsDOIOpen Access PDF

Abstract

A series of Mn(I) catalysts with readily accessible and more π-accepting phosphine-amino-phosphinite (P'(O)N(H)P) pincer ligands have been explored for the asymmetric transfer hydrogenation of aryl-alkyl ketones which led to good to high enantioselectivities (up to 98%) compared to other reported Mn-based catalysts for such reactions. The easy tunability of the chiral backbone and the phosphine moieties makes P'(O)N(H)P an alternative ligand framework to the well-known PNP-type pincers.

Topics & Concepts

PhosphineArylChemistryPincer movementEnantioselective synthesisAlkylPhosphiniteTransfer hydrogenationCatalysisLigand (biochemistry)Pincer ligandMedicinal chemistryStereochemistryOrganic chemistryCombinatorial chemistryRutheniumBiochemistryReceptorAsymmetric Hydrogenation and CatalysisChemical Synthesis and AnalysisSurface Chemistry and Catalysis
Mn(<scp>i</scp>) phosphine-amino-phosphinites: a highly modular class of pincer complexes for enantioselective transfer hydrogenation of aryl-alkyl ketones | Litcius