Аннотация:
Treatment of nucleobases, nucleosides, 5-membered N-heterocycles and terminal alkynes with trimethoxyvinylsilane in the presence of copper(II) acetate–TBAF system as catalyst affords the vinylation products.
Образец цитирования:
P. Arsenyan, A. Petrenko, E. Paegle, S. Belyakov, “Direct N- and C-vinylation with trimethoxyvinylsilane”, Mendeleev Commun., 21:6 (2011), 326–328
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2960
https://www.mathnet.ru/rus/mendc/v21/i6/p326
Эта публикация цитируется в следующих 12 статьяx:
Eleni Papaplioura, Maëva Mercier, Soufyan Jerhaoui, Michael Schnürch, “The Vinyl Group: Small but Mighty – Transition Metal Catalyzed and Non‐Catalyzed Vinylation Reactions”, ChemCatChem, 2024
Shou-Jie Shen, Le-Mei Wang, Guo-Mei Gong, Yan-Jiao Wang, Jin-Yan Liang, Jun-Wen Wang, “Construction of sulfur-containing N-vinylimides: N-addition of imides to propargyl sulfonium salts”, RSC Adv., 12:20 (2022), 12663
Fabio Juliá, Jiyao Yan, Fritz Paulus, Tobias Ritter, “Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene”, J. Am. Chem. Soc., 143:33 (2021), 12992
Elena Semina, Pavel Tuzina, Frank Bienewald, A. Stephen K. Hashmi, Thomas Schaub, “Ruthenium-catalyzed synthesis of vinylamides at low acetylene pressure”, Chem. Commun., 56:44 (2020), 5977
Konstantin Rodygin, Alexander Bogachenkov, Valentine Ananikov, “Vinylation of a Secondary Amine Core with Calcium Carbide for Efficient Post-Modification and Access to Polymeric Materials”, Molecules, 23:3 (2018), 648
М. С. Ледовская, В. В. Воронин, К. С. Родыгин, “Методы синтеза O-, S- и N-винильных производных”, Усп. хим., 87:2 (2018), 167–191; M. S. Ledovskaya, V. V. Voronin, K. S. Rodygin, “Methods for the synthesis of O-, S- and N-vinyl derivatives”, Russian Chem. Reviews, 87:2 (2018), 167–191
Eakkaphon Rattanangkool, Tirayut Vilaivan, Mongkol Sukwattanasinitt, Sumrit Wacharasindhu, “An Atom‐Economic Approach for Vinylation of Indoles and Phenols Using Calcium Carbide as Acetylene Surrogate”, Eur J Org Chem, 2016:25 (2016), 4347
Sophie Racine, Jérémy Vuilleumier, Jérôme Waser, “Nucleoside Analogues: Synthesis from Strained Rings”, Israel Journal of Chemistry, 56:6-7 (2016), 566
Ilona Domracheva, Ruslan Muhamadejev, Marina Petrova, Edvards Liepinsh, Anita Gulbe, Irina Shestakova, Gunars Duburs, Pavel Arsenyan, “1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) increases Carmofur stability and in vitro antiproliferative effect”, Toxicology Reports, 2 (2015), 377
Sophie Racine, Florian de Nanteuil, Eloisa Serrano, Jérôme Waser, “Synthesis of (Carbo)nucleoside Analogues by [3+2] Annulation of Aminocyclopropanes”, Angewandte Chemie, 126:32 (2014), 8624
Sophie Racine, Florian de Nanteuil, Eloisa Serrano, Jérôme Waser, “Synthesis of (Carbo)nucleoside Analogues by [3+2] Annulation of Aminocyclopropanes”, Angew Chem Int Ed, 53:32 (2014), 8484
Pavel Arsenyan, Alla Petrenko, Edgars Paegle, Sergey Belyakov, “ChemInform Abstract: Direct N‐ and C‐Vinylation with Trimethoxyvinylsilane.”, ChemInform, 43:16 (2012)