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Unlocking the Potential of Bio-Based Nitrogen-Rich Furanic Platforms as Biomass Synthons.
Gomes, Rafael F A; Gonçalves, Bruno M F; Andrade, Késsia H S; Sousa, Bárbara B; Maulide, Nuno; Bernardes, Gonçalo J L; Afonso, Carlos A M.
Afiliación
  • Gomes RFA; Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.
  • Gonçalves BMF; Yusuf Hamied Department of Chemistry, University of Cambridge, CB2 1EW, Cambridge, UK.
  • Andrade KHS; Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.
  • Sousa BB; Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.
  • Maulide N; Instituto de Medicina Molecular, João Lobo Antunes, Faculdade de Medicina da, Universidade de Lisboa, 1649-028, Lisboa, Portugal.
  • Bernardes GJL; Institute of Organic Chemistry, University of Vienna, 1090, Vienna, Austria.
  • Afonso CAM; Yusuf Hamied Department of Chemistry, University of Cambridge, CB2 1EW, Cambridge, UK.
Angew Chem Int Ed Engl ; 62(28): e202304449, 2023 07 10.
Article en En | MEDLINE | ID: mdl-37142557
The demand for new biomass-derived fine and commodity chemicals propels the discovery of new methodologies and synthons. Whereas furfural and 5-hydroxymethylfurfural are cornerstones of sustainable chemistry, 3-acetamido-5-acetyl furan (3A5AF), an N-rich furan obtained from chitin biomass, remains unexplored, due to the poor reactivity of the acetyl group relative to previous furanic aldehydes. Here we developed a reactive 3-acetamido-5-furfuryl aldehyde (3A5F) and demonstrated the utility of this synthon as a source of bio-derived nitrogen-rich heteroaromatics, carbocycles, and as a bioconjugation reagent.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Furaldehído / Furanos Idioma: En Revista: Angew Chem Int Ed Engl Año: 2023 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Furaldehído / Furanos Idioma: En Revista: Angew Chem Int Ed Engl Año: 2023 Tipo del documento: Article País de afiliación: Portugal