Keywords
alkyne hydration
catalysis
gold complexes
hydroamination
hydrohydrazination
N-heterocyclic carbenes
synthesis
Abstract
New gold (I) complexes with bulky fluorinated N-heterocyclic carbene ligands were synthesized and fully characterized. Their catalytic activity was tested in model reactions such as intramolecular hydroamination of 2-(phenylethynyl)aniline, alkyne hydration and hydrohydrazination of henylacetylene. In all studied cases new complexes demonstrated from good to excellent catalytic activities under standard conditions.
Funders
Russian Science Foundation
25-13-00209
References
1.
Valente C., Çalimsiz S., Hoi K.H., Mallik D., Sayah M., Organ M.G.
Angewandte Chemie - International Edition,
2012
2.
Fortman G.C., Nolan S.P.
Chemical Society Reviews,
2011
3.
Hopkinson M.N., Richter C., Schedler M., Glorius F.
Nature,
2014
4.
Chernenko A.Y., Shepelenko K.E., Minyaev M.E., Chernyshev V.M.
Mendeleev Communications,
2024
6.
Nasr A., Winkler A., Tamm M.
Coordination Chemistry Reviews,
2016
7.
Masoud S.M., Vorobyeva D.V., Petropavlovskikh D.A., Bruneau C., Osipov S.N.
Russian Chemical Reviews,
2021
8.
Iglesias-Sigüenza J., Izquierdo C., Díez E., Fernández R., Lassaletta J.M.
Dalton Transactions,
2016
9.
Reshi N.U., Bera J.K.
Coordination Chemistry Reviews,
2020
10.
Teixeira P., Bastin S., César V.
Israel Journal of Chemistry,
2022
11.
Mora M., Gimeno M.C., Visbal R.
Chemical Society Reviews,
2019
12.
Nayak S., Gaonkar S.L.
ChemMedChem,
2021
13.
Ansari E., Kumar R., Ratnam A.
Dalton Transactions,
2025
14.
Masoud S.M., Akmalov T.R., Palagin K.A., Dolgushin F.M., Nefedov S.E., Osipov S.N.
European Journal of Organic Chemistry,
2018
15.
Akmalov T.R., Masoud S.M., Vorobyeva D.V., Dolgushin F.M., Nefedov S.E., Osipov S.N.
Mendeleev Communications,
2019
16.
Azide-Alkyne Cycloaddition (CuAAC) in Alkane Solvents Catalyzed by Fluorinated NHC Copper(I) Complex
Topchiy M.A., Ageshina A.A., Gribanov P.S., Masoud S.M., Akmalov T.R., Nefedov S.E., Osipov S.N., Nechaev M.S., Asachenko A.F.
European Journal of Organic Chemistry,
2018
17.
Zhu S., Liang R., Chen L., Wang C., Ren Y., Jiang H.
Tetrahedron Letters,
2012
18.
Morozov O.S., Lunchev A.V., Bush A.A., Tukov A.A., Asachenko A.F., Khrustalev V.N., Zalesskiy S.S., Ananikov V.P., Nechaev M.S.
Chemistry - A European Journal,
2014
19.
Collado A., Gómez-Suárez A., Martin A.R., Slawin A.M., Nolan S.P.
Chemical Communications,
2013
20.
Topchiy M.A., Zotova M.A., Masoud S.M., Mailyan A.K., Ananyev I.V., Nefedov S.E., Asachenko A.F., Osipov S.N.
Chemistry - A European Journal,
2017
21.
Marinelli F., Arcadi A., Bianchi G.
Synthesis,
2004
22.
Mazzone G., Russo N., Sicilia E.
Organometallics,
2012
23.
Rzhevskiy S.A., Philippova A.N., Chesnokov G.A., Ageshina A.A., Minaeva L.I., Topchiy M.A., Nechaev M.S., Asachenko A.F.
Chemical Communications,
2021
24.
Cui D., Zheng J., Yang L., Zhang C.
Synlett,
2010
25.
Morozov O.S., Gribanov P.S., Asachenko A.F., Dorovatovskii P.V., Khrustalev V.N., Rybakov V.B., Nechaev M.S.
Advanced Synthesis and Catalysis,
2016
26.
Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A., Puschmann H.
Journal of Applied Crystallography,
2009
27.
Sheldrick G.M.
Acta Crystallographica Section A: Foundations and Advances,
2015
28.
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography,
2007