TY - JOUR
T1 - Preparation of chitosan-supported urea materials and their application in some organocatalytic procedures
AU - de Gonzalo, Gonzalo
AU - Franconetti, Antonio
AU - Fernández, Rosario
AU - Lassaletta, José M.
AU - Cabrera-Escribano, Francisca
PY - 2018/11/1
Y1 - 2018/11/1
N2 - © 2018 Elsevier Ltd An efficient and mild procedure was developed for the preparation of three chitosan-supported ureas containing electron-withdrawing groups. These catalysts were characterized and employed as organocatalysts in different transformations, including the enantioselective cyanosilylation of α-ketoesters and aldehydes, the asymmetric addition of formaldehyde tert-butyl hydrazone to prochiral α-ketoesters and a Friedel-Crafts reaction. Several parameters that can affect the activity and selectivity of the reactions were analysed. The supported catalysts can be reused for more than 10 cycles with only a small loss in their properties. Finally, theoretical DFT calculations were carried out to interpret the results of the catalysed reactions.
AB - © 2018 Elsevier Ltd An efficient and mild procedure was developed for the preparation of three chitosan-supported ureas containing electron-withdrawing groups. These catalysts were characterized and employed as organocatalysts in different transformations, including the enantioselective cyanosilylation of α-ketoesters and aldehydes, the asymmetric addition of formaldehyde tert-butyl hydrazone to prochiral α-ketoesters and a Friedel-Crafts reaction. Several parameters that can affect the activity and selectivity of the reactions were analysed. The supported catalysts can be reused for more than 10 cycles with only a small loss in their properties. Finally, theoretical DFT calculations were carried out to interpret the results of the catalysed reactions.
KW - 4-Chlorobenzaldehyde (PubChem CID: 7726)
KW - Acetophenone (PubChem CID: 7410)
KW - Benzaldehyde (PubChem CID: 240)
KW - Chiral tertiary alcohols
KW - Chitosan-supported ureas
KW - Cyanosilylation
KW - DFT calculations
KW - Ethyl 2-oxo-4-phenybutyrate (PubChem CID: 562087)
KW - Ethyl benzoylformate (PubChem CID: 15349)
KW - Heterogeneous catalysis
KW - Indole (PubChem CID: 798)
KW - Organocatalysis
KW - p-Nitrophenol (PubChem CID: 980)
KW - tert-Butylhydrazine hydrochloride (PubChem CID: 81889)
KW - trans-β-Nitrostyrene (PubChem CID: 5284459)
KW - Trimethylsilyl cyanide (PubChem CID: 82115)
UR - https://www.scopus.com/pages/publications/85049884871
U2 - 10.1016/j.carbpol.2018.07.009
DO - 10.1016/j.carbpol.2018.07.009
M3 - Article
C2 - 30143140
SN - 0144-8617
VL - 199
SP - 365
EP - 374
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
ER -