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Year Number of Results
2002 1
2010 1
2011 1
2015 1
2016 3
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2020 4
2021 4
2022 4
2023 3
2024 2

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24 results

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Page 1
Selective nickel-catalyzed fluoroalkylations of olefins.
Zhang S , Weniger F , Ye F , Rabeah J , Ellinger S , Zaragoza F , Taeschler C , Neumann H , Brückner A , Beller M . Zhang S , et al. Chem Commun (Camb). 2020 Dec 8;56(96):15157-15160. doi: 10.1039/d0cc06652d. Chem Commun (Camb). 2020. PMID: 33210679
Mild and selective nickel-catalyzed trifluoromethylation and perfluoroalkylation reactions of alkenes were developed to provide fluorinated olefins, including natural products, pharmaceuticals, and variety of synthetic building blocks in good to excellent yields (38 exampl …
Mild and selective nickel-catalyzed trifluoromethylation and perfluoroalkylation reactions of alkenes were developed to provide fluor …
Streamlining the synthesis of amides using Nickel-based nanocatalysts.
Gao J, Ma R, Poovan F, Zhang L, Atia H, Kalevaru NV, Sun W, Wohlrab S, Chusov DA, Wang N, Jagadeesh RV, Beller M. Gao J, et al. Nat Commun. 2023 Aug 17;14(1):5013. doi: 10.1038/s41467-023-40614-1. Nat Commun. 2023. PMID: 37591856 Free PMC article.
Here, we present a robust methodology for amide synthesis compared to traditional amidation reactions: the reductive amidation of esters with nitro compounds under additives-free conditions. In the presence of a specific heterogeneous nickel-based catalyst a wide range of …
Here, we present a robust methodology for amide synthesis compared to traditional amidation reactions: the reductive amidation of esters wit …
Heterogeneous nickel-catalysed reversible, acceptorless dehydrogenation of N-heterocycles for hydrogen storage.
Ryabchuk P , Agapova A , Kreyenschulte C , Lund H , Junge H , Junge K , Beller M . Ryabchuk P , et al. Chem Commun (Camb). 2019 Apr 23;55(34):4969-4972. doi: 10.1039/c9cc00918c. Chem Commun (Camb). 2019. PMID: 30968097
Nickel-based nanocatalysts were used in acceptorless, reversible dehydrogenation and hydrogenation reactions of N-heterocycles. ...This concept has been demonstrated in a continuous hydrogenation/dehydrogenation sequence of quinaldine with negligible loss in activity of th
Nickel-based nanocatalysts were used in acceptorless, reversible dehydrogenation and hydrogenation reactions of N-heterocycles. ...Th
Nickel as a co-catalyst for photocatalytic hydrogen evolution on graphitic-carbon nitride (sg-CN): what is the nature of the active species?
Indra A, Menezes PW, Kailasam K, Hollmann D, Schröder M, Thomas A, Brückner A, Driess M. Indra A, et al. Chem Commun (Camb). 2016 Jan 4;52(1):104-7. doi: 10.1039/c5cc07936e. Chem Commun (Camb). 2016. PMID: 26498497 Free article.
The nature of a nickel-based co-catalyst deposited on a sol-gel prepared porous graphitic-carbon nitride (sg-CN), for photocatalytic H2 production from water, has been investigated. ...
The nature of a nickel-based co-catalyst deposited on a sol-gel prepared porous graphitic-carbon nitride (sg-CN), for photocatalytic …
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst.
Lücke MP, Yao S, Driess M. Lücke MP, et al. Chem Sci. 2021 Jan 8;12(8):2909-2915. doi: 10.1039/d0sc06471h. Chem Sci. 2021. PMID: 34164057 Free PMC article.
Their reaction with Ni(cod)(2) (cod = cycloocta-1,5-diene) affords the corresponding 16 VE nickel(0) complexes with an intramolecular eta (2)-arene coordination of Ni, [E(Terp)E]Ni(eta (2)-arene) (E = P(III), Si(II); arene = phenylene spacer). ...With this system, the curr …
Their reaction with Ni(cod)(2) (cod = cycloocta-1,5-diene) affords the corresponding 16 VE nickel(0) complexes with an intramolecular …
An international Delphi consensus for surgical quality assessment of lymphadenectomy and anastomosis in minimally invasive total gastrectomy for gastric cancer.
Cizmic A, Romic I, Balla A, Barabino N, Anania G, Baiocchi GL, Bakula B, Balagué C, Berlth F, Bintintan V, Bracale U, Egberts JH, Fuchs HF, Gisbertz SS, Gockel I, Grimminger P, van Hillegersberg R, Inaki N, Immanuel A, Korr D, Lingohr P, Mascagni P, Melling N, Milone M, Mintz Y, Morales-Conde S, Moulla Y, Müller-Stich BP, Nakajima K, Nilsson M, Reeh M, Sileri P, Targarona EM, Ushimaru Y, Kim YW, Markar S, Nickel F, Mitra AT. Cizmic A, et al. Surg Endosc. 2024 Feb;38(2):488-498. doi: 10.1007/s00464-023-10614-9. Epub 2023 Dec 26. Surg Endosc. 2024. PMID: 38148401 Free PMC article.
Reductive amination using cobalt-based nanoparticles for synthesis of amines.
Murugesan K, Chandrashekhar VG, Senthamarai T, Jagadeesh RV, Beller M. Murugesan K, et al. Nat Protoc. 2020 Apr;15(4):1313-1337. doi: 10.1038/s41596-019-0258-z. Epub 2020 Mar 18. Nat Protoc. 2020. PMID: 32203487
Common catalysts used for reductive aminations, especially for the synthesis of primary amines, are based on precious metals or Raney nickel. However, their drawbacks and limited applicability inspired us to look for alternative catalysts. ...
Common catalysts used for reductive aminations, especially for the synthesis of primary amines, are based on precious metals or Raney nic
Implementing governmental oversight of enhanced potential pandemic pathogen research.
Ebright RH, MacIntyre R, Dudley JP, Butler CD, Goffinet A, Hammond E, Harris ED, Kakeya H, Lambrinidou Y, Leitenberg M, Newman SA, Nickels BE, Rahalkar MC, Ridley MW, Salzberg SL, Seshadri H, Theißen G, VanDongen AM, Washburne A. Ebright RH, et al. J Virol. 2024 Apr 16;98(4):e0023724. doi: 10.1128/jvi.00237-24. Epub 2024 Mar 13. J Virol. 2024. PMID: 38477586 Free PMC article. No abstract available.
24 results