Efficient and chemoselective hydrogenation of aldehydes catalyzed by a well-defined PN3 -pincer manganese (II) catalyst precursor: an application in furfural conversion
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ArticleAuthors
Huang, Kuo-Wei
Gholap, Sandeep S.
Al Dakhil, Abdullah

Chakraborty, Priyanka
Li, Huaifeng

Dutta, Indranil

Das, Pradip
KAUST Department
Chemical Science ProgramHomogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Date
2021Submitted Date
2021-08-28Permanent link to this record
http://hdl.handle.net/10754/672890
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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=C double bond/CΞC triple bond intact. Our methodology was demonstrated for biomass derived feedstock such as furfural and 2,5-diformyl furfural to furfuryl alcohol and 2-hydroxy furfuryl alcohol respectively.Citation
Huang, K.-W., Gholap, S. S., Al-Dakhil, A., Chakraborty, P., Li, H., Dutta, I., & Das, P. (2021). Efficient and chemoselective hydrogenation of aldehydes catalyzed by a well-defined PN3 -pincer manganese (II) catalyst precursor: an application in furfural conversion. Chemical Communications. doi:10.1039/d1cc04808bSponsors
This work was supported by King Abdullah University of Science and Technology (KAUST).Publisher
Royal Society of Chemistry (RSC)Journal
Chemical CommunicationsAdditional Links
http://pubs.rsc.org/en/Content/ArticleLanding/2021/CC/D1CC04808Bae974a485f413a2113503eed53cd6c53
10.1039/d1cc04808b
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