Issue 89, 2021

Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN3–pincer manganese(ii) catalyst precursors: an application in furfural conversion

Abstract

Well-defined and air-stable PN3–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[double bond, length as m-dash]C double bond/C[triple bond, length as m-dash]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.

Graphical abstract: Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN3–pincer manganese(ii) catalyst precursors: an application in furfural conversion

Supplementary files

Article information

Article type
Communication
Submitted
28 Aug 2021
Accepted
14 Oct 2021
First published
15 Oct 2021
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2021,57, 11815-11818

Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN3–pincer manganese(II) catalyst precursors: an application in furfural conversion

S. S. Gholap, A. A. Dakhil, P. Chakraborty, H. Li, I. Dutta, P. K. Das and K. Huang, Chem. Commun., 2021, 57, 11815 DOI: 10.1039/D1CC04808B

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