Cellulose/β-cyclodextrin hydrogel supported metal nanoparticles as recyclable catalysts in the 4-nitrophenol reduction, Suzuki–Miyaura coupling and click reactions

[1] Astruc D(2020)Introduction: nanoparticles in catalysis Chem Rev 120 461-463

[2] Baran NY(2018)Production of novel palladium nanocatalyst stabilized with sustainable chitosan/cellulose composite and its catalytic performance in Suzuki–Miyaura coupling reactions Carbohydr Polym 181 596-604

[3] Baran T(2018)A new air and moisture stable robust bio-polymer based palladium catalyst for highly efficient synthesis of biaryl compounds Appl Organomet Chem 2 e4076-116

[4] Mentes A(2016)Microwave assisted synthesis of biarlys by C–C coupling reactions with a new chitosan supported Pd(II) catalyst J Mol Struct 1122 111-221

[5] Baran T(2016)An environmental catalyst derived from biological waste materials for green synthesis of biaryls via Suzuki coupling reactions J Mol Catal A Chem 420 216-113

[6] Baran NY(2018)Production of magnetically recoverable, thermally stable, bio-based catalyst: remarkable turnover frequency and reusability in Suzuki coupling reaction Chem Eng J 331 102-2541

[7] Mentes A(2016)An efficient and recyclable thiourea-supported copper(I) chloride catalyst for azide–alkyne cycloaddition reactions Green Chem 18 2534-175

[8] Baran T(2018)3D-macroporous chitosan-based scaffolds with in situ formed Pd and Pt nanoparticles for nitrophenol reduction Carbohydr Polym 192 166-189

[9] Mentes A(2006)Unique gelation behavior of cellulose in NaOH/Urea aqueous solution Biomacromol 7 183-4493

[10] Baran T(2022)Design of a palladium nanocatalyst produced from schiff base modified dialdehyde cellulose and its application in aryl halide cyanation and reduction of nitroarenes Cellulose 29 4475-3983

[1] Astruc D(2020)Introduction: nanoparticles in catalysis Chem Rev 120 461-463

[2] Baran NY(2018)Production of novel palladium nanocatalyst stabilized with sustainable chitosan/cellulose composite and its catalytic performance in Suzuki–Miyaura coupling reactions Carbohydr Polym 181 596-604

[3] Baran T(2018)A new air and moisture stable robust bio-polymer based palladium catalyst for highly efficient synthesis of biaryl compounds Appl Organomet Chem 2 e4076-116

[4] Mentes A(2016)Microwave assisted synthesis of biarlys by C–C coupling reactions with a new chitosan supported Pd(II) catalyst J Mol Struct 1122 111-221

[5] Baran T(2016)An environmental catalyst derived from biological waste materials for green synthesis of biaryls via Suzuki coupling reactions J Mol Catal A Chem 420 216-113

[6] Baran NY(2018)Production of magnetically recoverable, thermally stable, bio-based catalyst: remarkable turnover frequency and reusability in Suzuki coupling reaction Chem Eng J 331 102-2541

[7] Mentes A(2016)An efficient and recyclable thiourea-supported copper(I) chloride catalyst for azide–alkyne cycloaddition reactions Green Chem 18 2534-175

[8] Baran T(2018)3D-macroporous chitosan-based scaffolds with in situ formed Pd and Pt nanoparticles for nitrophenol reduction Carbohydr Polym 192 166-189

[9] Mentes A(2006)Unique gelation behavior of cellulose in NaOH/Urea aqueous solution Biomacromol 7 183-4493

[10] Baran T(2022)Design of a palladium nanocatalyst produced from schiff base modified dialdehyde cellulose and its application in aryl halide cyanation and reduction of nitroarenes Cellulose 29 4475-3983