Decorated palladium nanoparticles on mesoporous organosilicate as an efficient catalyst for Sonogashira coupling reaction

[1] Astruc D(2005)Nanoparticles as recyclable catalysts: the frontier between homogeneous and heterogeneous catalysis Angew. Chem. Int. Ed. 44 7852-7872

[2] Lu F(2016)Sustainable approach to waste-minimized sonogashira cross-coupling reaction based on recoverable/reusable heterogeneous catalytic/base system and acetonitrile azeotrope ACS Sustain Chem. Eng. 4 7209-7216

[3] Aranzaes JR(2005)Palladium-catalyzed cross-coupling reactions in total synthesis Angew. Chem. Int. Ed. 44 4442-4489

[4] Kozell V(1998)Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores Science 279 548-1635

[5] McLaughlin M(2020)The synthesis of SBA-15-Pr-3AP@Pd and its application as a highly dynamic, ecofriendly heterogeneous catalyst for Suzuki-Miyaura cross-coupling reaction Res. Chem. Intermed. 25 1614-28248

[6] Strappaveccia G(2019)Development of sulfonic-acid-functionalized mesoporous materials: synthesis and catalytic applications Chem. Eur. J. 4 28238-5121

[7] Santoro S(2014)Nanoporous silica-supported organocatalyst: a heterogeneous and green hybrid catalyst for organic transformations RSC Adv. 40 5084-3160

[8] Bivona LA(2011)Recent advances in Sonogashira reactions Chem. Soc. Rev. 28 3152-5755

[9] Aprile C(2009)Conformational control of metallocene backbone by cyclopentadienyl ring substitution: a new concept in polyphosphane ligands evidenced by “through-space” nuclear spin − spin coupling. Application in heteroaromatics arylation by direct C − H activation Organometallics 69 5752-12

[10] Gruttadauria M(2004)Ligand-, copper-, and amine-free sonogashira reaction of aryl iodides and bromides with terminal alkynes J. Org. Chem. 853 5-15742

[1] Astruc D(2005)Nanoparticles as recyclable catalysts: the frontier between homogeneous and heterogeneous catalysis Angew. Chem. Int. Ed. 44 7852-7872

[2] Lu F(2016)Sustainable approach to waste-minimized sonogashira cross-coupling reaction based on recoverable/reusable heterogeneous catalytic/base system and acetonitrile azeotrope ACS Sustain Chem. Eng. 4 7209-7216

[3] Aranzaes JR(2005)Palladium-catalyzed cross-coupling reactions in total synthesis Angew. Chem. Int. Ed. 44 4442-4489

[4] Kozell V(1998)Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores Science 279 548-1635

[5] McLaughlin M(2020)The synthesis of SBA-15-Pr-3AP@Pd and its application as a highly dynamic, ecofriendly heterogeneous catalyst for Suzuki-Miyaura cross-coupling reaction Res. Chem. Intermed. 25 1614-28248

[6] Strappaveccia G(2019)Development of sulfonic-acid-functionalized mesoporous materials: synthesis and catalytic applications Chem. Eur. J. 4 28238-5121

[7] Santoro S(2014)Nanoporous silica-supported organocatalyst: a heterogeneous and green hybrid catalyst for organic transformations RSC Adv. 40 5084-3160

[8] Bivona LA(2011)Recent advances in Sonogashira reactions Chem. Soc. Rev. 28 3152-5755

[9] Aprile C(2009)Conformational control of metallocene backbone by cyclopentadienyl ring substitution: a new concept in polyphosphane ligands evidenced by “through-space” nuclear spin − spin coupling. Application in heteroaromatics arylation by direct C − H activation Organometallics 69 5752-12

[10] Gruttadauria M(2004)Ligand-, copper-, and amine-free sonogashira reaction of aryl iodides and bromides with terminal alkynes J. Org. Chem. 853 5-15742