28. Zhang J, Lu G, Cai C (2016) Chemoselective transfer hydrogenation of nitroarenes by highly
dispersed Ni-Co BMNPs. Catal Commun 84:25–29. https://doi.org/10.1016/j.catcom.2016.
05.023
29. Bódis J, Lefferts L, Müller TE, Pestman R, Lercher JA (2005) Activity and selectivity control
in reductive amination of butyraldehyde over noble metal catalysts. Catal Lett 104:23–28.
https://doi.org/10.1007/s10562-005-7431-4
30. Alonso F, Riente P, Yus M (2008) Hydrogen-transfer reductive amination of aldehydes
catalysed by nickel nanoparticles. Synlett:1289–1292. https://doi.org/10.1055/s-20081072748
31. Jagadeesh R, Murugesan K, Beller M (2019) Reusable nickel nanoparticles-catalyzed reductive amination for selective synthesis of primary amines. Angew Chem Int Ed. https://doi.org/
10.1002/anie.201812100
32. Sharma RK, Yadav M, Gaur R, Monga Y, Adholeya A (2015) Magnetically retrievable silicabased nickel nanocatalyst for Suzuki–Miyaura cross-coupling reaction. Cat Sci Technol
5:2728–2740. https://doi.org/10.1039/C4CY01736F
33. Handa S, Slack ED, Lipshutz BH (2015) Nanonickel-catalyzed Suzuki–Miyaura crosscouplings in water. Angew Chem Int Ed 54:11994–11998. https://doi.org/10.1002/anie.
201505136
34. Sankar M, Dimitratos N, Miedziak PJ, Wells PP, Kiely CJ, Hutchings GJ (2012)
Designing bimetallic catalysts for a green and sustainable future. Chem Soc Rev
41:8099–8139. https://doi.org/10.1039/C2CS35296F
35. Liu H, Mei Q, Li S, Yang Y, Wang Y, Liu H, Zheng L, An P, Zhang J, Han B (2018)
Selective hydrogenation of unsaturated aldehydes over Pt nanoparticles promoted by the
cooperation of steric and electronic effects. Chem Commun 54:908–911. https://doi.org/10.
1039/C7CC08942B
36. Jang J, Byun S, Kim BM, Lee S (2018) Arylsilylation of aryl halides using the magnetically
recyclable bimetallic Pd–Pt–Fe3O4 catalyst. Chem Commun 54:3492–3495. https://doi.org/
10.1039/C7CC09926F
37. Heiss C, Schlosser M (2003) Organometallic control over the regiospecificity of
functionalization reactions: 1,2,3-trifluorobenzene and bromo derivatives thereof as substrates.
Eur J Org Chem 2003:447–451. https://doi.org/10.1002/ejoc.200390078
38. Luliński S, Serwatowski J (2003) Regiospecific metalation of oligobromobenzenes. J Org
Chem 68:5384–5387. https://doi.org/10.1021/jo0340511
39. Zeng J (2012) A simple eco-friendly solution phase reduction method for the synthesis
of polyhedra platinum nanoparticles with high catalytic activity for methanol electrooxidation.
J Mater Chem 22:3170–3176. https://doi.org/10.1039/C1JM14413H
40. Pitre SP, Scaiano JC, Yoon TP (2017) Photocatalytic Indole Diels–Alder cycloadditions
mediated by heterogeneous platinum-modified titanium dioxide. ACS Catal 7:6440–6444.
https://doi.org/10.1021/acscatal.7b02223
41. Zamani A, Poursattar Marjani A, Nikoo A, Heidarpour M, Dehghan A (2018) Synthesis and
characterization of copper nanoparticles on walnut shell for catalytic reduction and C-C
coupling reaction. Inorg Nano-Met Chem 48:176–181. https://doi.org/10.1080/24701556.
2018.1503676
42. He J, Zhang M, Primo A, García H, Li Z (2018) Selective photocatalytic benzene
hydroxylation to phenol using surface-modified Cu 2 O supported on graphene. J Mater
Chem A 6:19782–19787. https://doi.org/10.1039/C8TA07095D
43. Rostovtsev VV, Green LG, Fokin VV, Sharpless KB (2002) A stepwise huisgen cycloaddition
process: copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes. Angew
Chem Int Ed 41:2596–2599. https://doi.org/10.1002/1521-3773(20020715)41:14<2596::
AID-ANIE2596>3.0.CO;2-4
44. Tornøe CW, Christensen C, Meldal M (2002) Peptidotriazoles on solid phase: [1,2,3]-triazoles
by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.
J Org Chem 67:3057–3064. https://doi.org/10.1021/jo011148j
45. Alonso F, Moglie Y, Radivoy G (2015) Copper nanoparticles in click chemistry. Acc Chem
Res 48:2516–2528. https://doi.org/10.1021/acs.accounts.5b00293
124
M. Cortes-Clerget et al.
dispersed Ni-Co BMNPs. Catal Commun 84:25–29. https://doi.org/10.1016/j.catcom.2016.
05.023
29. Bódis J, Lefferts L, Müller TE, Pestman R, Lercher JA (2005) Activity and selectivity control
in reductive amination of butyraldehyde over noble metal catalysts. Catal Lett 104:23–28.
https://doi.org/10.1007/s10562-005-7431-4
30. Alonso F, Riente P, Yus M (2008) Hydrogen-transfer reductive amination of aldehydes
catalysed by nickel nanoparticles. Synlett:1289–1292. https://doi.org/10.1055/s-20081072748
31. Jagadeesh R, Murugesan K, Beller M (2019) Reusable nickel nanoparticles-catalyzed reductive amination for selective synthesis of primary amines. Angew Chem Int Ed. https://doi.org/
10.1002/anie.201812100
32. Sharma RK, Yadav M, Gaur R, Monga Y, Adholeya A (2015) Magnetically retrievable silicabased nickel nanocatalyst for Suzuki–Miyaura cross-coupling reaction. Cat Sci Technol
5:2728–2740. https://doi.org/10.1039/C4CY01736F
33. Handa S, Slack ED, Lipshutz BH (2015) Nanonickel-catalyzed Suzuki–Miyaura crosscouplings in water. Angew Chem Int Ed 54:11994–11998. https://doi.org/10.1002/anie.
201505136
34. Sankar M, Dimitratos N, Miedziak PJ, Wells PP, Kiely CJ, Hutchings GJ (2012)
Designing bimetallic catalysts for a green and sustainable future. Chem Soc Rev
41:8099–8139. https://doi.org/10.1039/C2CS35296F
35. Liu H, Mei Q, Li S, Yang Y, Wang Y, Liu H, Zheng L, An P, Zhang J, Han B (2018)
Selective hydrogenation of unsaturated aldehydes over Pt nanoparticles promoted by the
cooperation of steric and electronic effects. Chem Commun 54:908–911. https://doi.org/10.
1039/C7CC08942B
36. Jang J, Byun S, Kim BM, Lee S (2018) Arylsilylation of aryl halides using the magnetically
recyclable bimetallic Pd–Pt–Fe3O4 catalyst. Chem Commun 54:3492–3495. https://doi.org/
10.1039/C7CC09926F
37. Heiss C, Schlosser M (2003) Organometallic control over the regiospecificity of
functionalization reactions: 1,2,3-trifluorobenzene and bromo derivatives thereof as substrates.
Eur J Org Chem 2003:447–451. https://doi.org/10.1002/ejoc.200390078
38. Luliński S, Serwatowski J (2003) Regiospecific metalation of oligobromobenzenes. J Org
Chem 68:5384–5387. https://doi.org/10.1021/jo0340511
39. Zeng J (2012) A simple eco-friendly solution phase reduction method for the synthesis
of polyhedra platinum nanoparticles with high catalytic activity for methanol electrooxidation.
J Mater Chem 22:3170–3176. https://doi.org/10.1039/C1JM14413H
40. Pitre SP, Scaiano JC, Yoon TP (2017) Photocatalytic Indole Diels–Alder cycloadditions
mediated by heterogeneous platinum-modified titanium dioxide. ACS Catal 7:6440–6444.
https://doi.org/10.1021/acscatal.7b02223
41. Zamani A, Poursattar Marjani A, Nikoo A, Heidarpour M, Dehghan A (2018) Synthesis and
characterization of copper nanoparticles on walnut shell for catalytic reduction and C-C
coupling reaction. Inorg Nano-Met Chem 48:176–181. https://doi.org/10.1080/24701556.
2018.1503676
42. He J, Zhang M, Primo A, García H, Li Z (2018) Selective photocatalytic benzene
hydroxylation to phenol using surface-modified Cu 2 O supported on graphene. J Mater
Chem A 6:19782–19787. https://doi.org/10.1039/C8TA07095D
43. Rostovtsev VV, Green LG, Fokin VV, Sharpless KB (2002) A stepwise huisgen cycloaddition
process: copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes. Angew
Chem Int Ed 41:2596–2599. https://doi.org/10.1002/1521-3773(20020715)41:14<2596::
AID-ANIE2596>3.0.CO;2-4
44. Tornøe CW, Christensen C, Meldal M (2002) Peptidotriazoles on solid phase: [1,2,3]-triazoles
by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.
J Org Chem 67:3057–3064. https://doi.org/10.1021/jo011148j
45. Alonso F, Moglie Y, Radivoy G (2015) Copper nanoparticles in click chemistry. Acc Chem
Res 48:2516–2528. https://doi.org/10.1021/acs.accounts.5b00293
124
M. Cortes-Clerget et al.