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Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN<sup>3</sup>–pincer manganese(<scp>ii</scp>) catalyst precursors: an application in furfural conversion

Sandeep Suryabhan Gholap, Abdullah Al-Dakhil, Priyanka Chakraborty, Huaifeng Li, Indranil Dutta, Pradip Das, Kuo‐Wei Huang

2021Chemical Communications14 citationsDOIOpen Access PDF

Abstract

-pincer manganese(II) complexes were synthesized and used for the hydrogenation of aldehydes into alcohols under mild conditions using MeOH as a solvent. This protocol is applicable for a wide range of aldehydes containing various functional groups. Importantly, α,β-unsaturated aldehydes, including ynals, are hydrogenated with the CC double bond/CC triple bond intact. Our methodology was demonstrated for the conversion of biomass derived feedstocks such as furfural and 5-formylfurfural to furfuryl alcohol and 5-(hydroxymethyl)furfuryl alcohol respectively.

Topics & Concepts

FurfuralFurfuryl alcoholChemistryPincer movementCatalysisManganeseHydroxymethylOrganic chemistryAlcoholSolventBiomass (ecology)Triple bondDouble bondMedicinal chemistryOceanographyGeologyCatalysis for Biomass ConversionCatalysis and Hydrodesulfurization StudiesAsymmetric Hydrogenation and Catalysis
Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN<sup>3</sup>–pincer manganese(<scp>ii</scp>) catalyst precursors: an application in furfural conversion | Litcius