Аннотация:
Hydroamination of terminal alkynes with anilines in the presence of (C6F5)3PAuNTf2 catalyst affords 2-aryliminoalkanes whose reduction in situ with sodium borohydride gives the corresponding secondary amines in high yields.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
M. V. Anokhin, A. V. Murashkina, A. D. Averin, I. P. Beletskaya, “Simple and efficient AuI-based catalyst for hydroamination of alkynes”, Mendeleev Commun., 24:6 (2014), 332–333
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2569
https://www.mathnet.ru/rus/mendc/v24/i6/p332
Эта публикация цитируется в следующих 10 статьяx:
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И. П. Белецкая, C. Nájera, M. Yus, “Kaтaлиз и peгиoceлeктивнocть в peaкцияx гидpoфyнкциoнaлизaции yглepoдныx кpaтныx cвязeй. Чacть II. Гидpoaминиpoвaниe”, Усп. хим., 89:10 (2020), 1074–1114; I. P. Beletskaya, C. Nájera, M. Yus, “Catalysis and regioselectivity in hydrofunctionalization reactions of unsaturated carbon bonds. Part II. Hydroamination”, Russian Chem. Reviews, 89:10 (2020), 1074–1114
Yongsheng Chen, Sensheng Liu, Peng Cui, Yin Zhang, Qixing Liu, Haifeng Zhou, “Metal-free one-pot three-step process for the direct conversion of aryl alkynes into secondary amines with TfOH/B2(OH)4”, Tetrahedron Letters, 60:3 (2019), 327
L. A. Grishchenko, L. N. Parshina, V. V. Kireeva, B. A. Trofimov, “Gold-Catalyzed Nucleophilic Addition of Imidazole to Arabinogalactan Propargyl Ether”, Russ J Org Chem, 54:1 (2018), 154
A. I. Konovalov, I. S. Antipin, V. A. Burilov, T. I. Madzhidov, A. R. Kurbangalieva, A. V. Nemtarev, S. E. Solovieva, I. I. Stoikov, V. A. Mamedov, L. Ya. Zakharova, E. L. Gavrilova, O. G. Sinyashin, I. A. Balova, A. V. Vasilyev, I. G. Zenkevich, M. Yu. Krasavin, M. A. Kuznetsov, A. P. Molchanov, M. S. Novikov, V. A. Nikolaev, L. L. Rodina, A. F. Khlebnikov, I. P. Beletskaya, S. Z. Vatsadze, S. P. Gromov, N. V. Zyk, A. T. Lebedev, D. A. Lemenovskii, V. S. Petrosyan, V. G. Nenaidenko, V. V. Negrebetskii, Yu. I. Baukov, T. A. Shmigol', A. A. Korlyukov, A. S. Tikhomirov, A. E. Shchekotikhin, V. F. Traven', L. G. Voskresenskii, F. I. Zubkov, O. A. Golubchikov, A. S. Semeikin, D. B. Berezin, P. A. Stuzhin, V. D. Filimonov, E. A. Krasnokutskaya, A. Yu. Fedorov, A. V. Nyuchev, V. Yu. Orlov, R. S. Begunov, A. I. Rusakov, A. V. Kolobov, E. R. Kofanov, O. V. Fedotova, A. Yu. Egorova, V. N. Charushin, O. N. Chupakhin, Yu. N. Klimochkin, V. A. Osyanin, A. N. Reznikov, A. S. Fisyuk, G. , “Modern Trends of Organic Chemistry in Russian Universities”, Russ J Org Chem, 54:2 (2018), 157
Haifeng Yang, François P. Gabbaı̈, “Activation of a Hydroamination Gold Catalyst by Oxidation of a Redox-Noninnocent Chlorostibine Z-Ligand”, J. Am. Chem. Soc., 137:41 (2015), 13425
Ji Young Lee, Shin-Geol Kang, Chee-Hun Kwak, “Reaction of primary amines with N -ethynyl pendant arms attached to macrocyclic nickel(II) and copper(II) complexes: Formation of the complexes with pendant imine group(s)”, Inorganica Chimica Acta, 430 (2015), 61
Maksim V. Anokhin, Arina V. Murashkina, Alexei D. Averin, Irina P. Beletskaya, “ChemInform Abstract: Simple and Efficient AuI‐Based Catalyst for Hydroamination of Alkynes.”, ChemInform, 46:17 (2015)
M. V. Moskalev, A. A. Skatova, V. A. Chudakova, N. M. Khvoinova, N. L. Bazyakina, A. G. Morozov, O. V. Kazarina, A. V. Cherkasov, G. A. Abakumov, I. L. Fedushkin, “Hydroamination of alkynes with aromatic amines catalyzed by digallane (dpp-bian)Ga—Ga(dpp-bian)”, Russ Chem Bull, 64:12 (2015), 2830
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