| Literature DB >> 31531965 |
João M J M Ravasco1, Carlos M Monteiro1, Filipa Siopa1, Alexandre F Trindade1,2, Julie Oble3, Giovanni Poli3, Svilen P Simeonov4,5, Carlos A M Afonso1.
Abstract
A new chemoselective (enzymatic desymmetrization/Ru-catalyzed C-H activation) sequence to obtain differently substituted furans from the largely available 2,5-furandicarboxylic acid (FDCA) was developed. Series of di- and trisubstituted furans were prepared in very good yields and excellent chemoselectivity. This study discloses a new approach towards valorization of the furanics platform through the use of FDCA as a stable intermediate, thus circumventing the chemical instability of the parent 5-hydroxymethylfurfural.Entities:
Keywords: C−H activation; biocatalysis; biomass; continuous flow; furanic platform
Year: 2019 PMID: 31531965 DOI: 10.1002/cssc.201902051
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928