Skip to Main content Skip to Navigation
Journal articles

New functionalized scaffolds from hydroxymethylfurfural and glucosyloxymethylfurfural by Morita-Baylis-Hillman reaction with cycloalkenones

Lianjie Wang 1 Tan Jianeng 1 Mohammed Ahmar 1 Yves Queneau 1
1 COB - Chimie Organique et Bioorganique
ICBMS - Institut de Chimie et Biochimie Moléculaires et Supramoléculaires
Abstract : New highly functionalized scaffolds, namely 2-(2-furyl)hydroxymethyl-2-cycloalkenones, are reported. The access to these systems is one step using an aqueous Morita–Baylis–Hillman reaction combining hydroxymethylfurfural and glucosyloxymethylfurfural and cycloalkenones for which the reaction conditions (promoter, solvent, concentration, and stoichiometry) have been optimized.
Document type :
Journal articles
Complete list of metadatas

Cited literature [83 references]  Display  Hide  Download

https://hal-udl.archives-ouvertes.fr/hal-02285351
Contributor : Umr5246 Icbms <>
Submitted on : Thursday, July 16, 2020 - 4:58:55 PM
Last modification on : Thursday, July 16, 2020 - 6:05:16 PM

File

CR Chimie 2019 revised.pdf
Files produced by the author(s)

Identifiers

Citation

Lianjie Wang, Tan Jianeng, Mohammed Ahmar, Yves Queneau. New functionalized scaffolds from hydroxymethylfurfural and glucosyloxymethylfurfural by Morita-Baylis-Hillman reaction with cycloalkenones. Comptes Rendus Chimie, Elsevier Masson, 2019, 22 (9-10), pp.615-620. ⟨10.1016/j.crci.2019.09.002⟩. ⟨hal-02285351⟩

Share

Metrics

Record views

98

Files downloads

57