5-hydroxymethylfurfural and cyclopentanone

5-hydroxymethylfurfural has been researched along with cyclopentanone* in 2 studies

Other Studies

2 other study(ies) available for 5-hydroxymethylfurfural and cyclopentanone

Article	Year
Cyclopentanone Derivatives from 5-Hydroxymethylfurfural via 1-Hydroxyhexane-2,5-dione as Intermediate. ChemSusChem, 2018, 01-23, Volume: 11, Issue:2 An efficient strategy for the conversion of biomass derived 5-hydroxymethylfurfural (HMF) into 2-hydroxy-3-methylcyclopent-2-enone (MCP) by an intramolecular aldol condensation of 1-hydroxyhexane-2,5-dione (HHD) has been developed. Further transformations of MCP towards the diol, enol acetate, levulinic acid and N-heterocyclic compounds are also reported. Topics: Biomass; Catalysis; Cyclopentanes; Furaldehyde; Hexanes; Hydrogen Bonding; Models, Molecular; X-Ray Diffraction	2018
Conversion of 5-hydroxymethylfurfural to a cyclopentanone derivative by ring rearrangement over supported Au nanoparticles. Chemical communications (Cambridge, England), 2014, May-30, Volume: 50, Issue:42 Supported Au nanoparticles showed efficient catalytic performance for the ring rearrangement of 5-hydroxymethylfurfural (HMF) to a cyclopentanone derivative, 3-hydroxymethylcyclopentanone (HCPN), by taking advantage of the selective hydrogenation on Au nanoparticles and the Lewis acid catalysis of metal oxide supports. Among various metal oxide supported Au catalysts, the highest yield of HCPN was obtained by using Au/Nb2O5 (86% yield). Topics: Cyclopentanes; Furaldehyde; Gold; Metal Nanoparticles	2014

Article

Year

Cyclopentanone Derivatives from 5-Hydroxymethylfurfural via 1-Hydroxyhexane-2,5-dione as Intermediate.

ChemSusChem, 2018, 01-23, Volume: 11, Issue:2

An efficient strategy for the conversion of biomass derived 5-hydroxymethylfurfural (HMF) into 2-hydroxy-3-methylcyclopent-2-enone (MCP) by an intramolecular aldol condensation of 1-hydroxyhexane-2,5-dione (HHD) has been developed. Further transformations of MCP towards the diol, enol acetate, levulinic acid and N-heterocyclic compounds are also reported.

Topics: Biomass; Catalysis; Cyclopentanes; Furaldehyde; Hexanes; Hydrogen Bonding; Models, Molecular; X-Ray Diffraction

2018

Conversion of 5-hydroxymethylfurfural to a cyclopentanone derivative by ring rearrangement over supported Au nanoparticles.

Chemical communications (Cambridge, England), 2014, May-30, Volume: 50, Issue:42

Supported Au nanoparticles showed efficient catalytic performance for the ring rearrangement of 5-hydroxymethylfurfural (HMF) to a cyclopentanone derivative, 3-hydroxymethylcyclopentanone (HCPN), by taking advantage of the selective hydrogenation on Au nanoparticles and the Lewis acid catalysis of metal oxide supports. Among various metal oxide supported Au catalysts, the highest yield of HCPN was obtained by using Au/Nb2O5 (86% yield).

Topics: Cyclopentanes; Furaldehyde; Gold; Metal Nanoparticles

2014