Аннотация:
The reaction of 3-(trimethylsilyl)propynal, 3-(triethylgermyl) propynal or 3-phenylpropynal with tosylmethyl isocyanide affords new 5-alkynyl-4-tosyl-2-oxazolines and/or 5-alkynyl-1,3-oxazoles.
Образец цитирования:
V. G. Elshina, V. V. Novokshonov, E. A. Verochkina, I. A. Ushakov, I. B. Rosentsveig, N. V. Vchislo, “Synthesis of oxazolines and oxazoles by the reaction of propynals with tosylmethyl isocyanide”, Mendeleev Commun., 29:6 (2019), 651–652
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1618
https://www.mathnet.ru/rus/mendc/v29/i6/p651
Эта публикация цитируется в следующих 11 статьяx:
B. A. Trofimov, E. Yu. Schmidt, “Unknown chemistry of acetylene: one-year achievements”, Russ Chem Bull, 73:7 (2024), 1866
Maxim D. Gotsko, Ivan V. Saliy, Igor A. Ushakov, Lyubov N. Sobenina, Boris A. Trofimov, “Functionalized 2,3′-Bipyrroles and Pyrrolo[1,2-c]imidazoles from Acylethynylpyrroles and Tosylmethylisocyanide”, Molecules, 29:4 (2024), 885
Nadezhda V. Vchislo, Victoria G. Fedoseeva, Ekaterina A. Verochkina, “The Reactions of p-Tosylmethyl Isocyanide with Aldehydes in the Synthesis
of Heterocyclic Compounds: A Review”, MROC, 20:4 (2023), 372
Nadezhda V. Vchislo, Ekaterina A. Verochkina, Victoria G. Fedoseeva, “Synthesis of alkenyl- and alkynyloxazoles and –oxazolines using tosylmethyl isocyanide as a key building block (microreview)”, Chem Heterocycl Comp, 59:8 (2023), 537
Yuting Wan, Jieqing Wu, Hongfei Ma, Hongjun Zhu, Patrick J. Walsh, Yufeng Li, “Copper(i)-catalyzed tandem synthesis of 4,5-functionalized oxazoles from isocyanoacetate and aldehydes”, New J. Chem., 46:35 (2022), 16840
K. T. Ibrahim, Mohan Neetha, Gopinathan Anilkumar, “Advancements in the synthesis of oxazolines”, Monatsh Chem, 153:10 (2022), 837
Maxim D. Gotsko, Ivan V. Saliy, Lyubov' N. Sobenina, Igor A. Ushakov, Boris A. Trofimov, “Tosyl/pyrrolyl-capped 1,3-enynes via t-BuOK-assisted reaction of TosMIC with acylethynylpyrroles: a new feature of this popular reagent”, New J. Chem., 46:35 (2022), 16646
Franca M. Cordero, Luisa Lascialfari, Fabrizio Machetti, Progress in Heterocyclic Chemistry, 32, 2021, 365
Ivan V. Saliy, Maxim D. Gotsko, Lyubov' N. Sobenina, Igor A. Ushakov, Boris A. Trofimov, “Chemo- and stereoselective synthesis of E-2-(2-acyl-1-tosylvinyl)pyrroles from tosylmethyl isocyanide (TosMIC) and 2-(acylethynyl)pyrroles”, Tetrahedron Letters, 84 (2021), 153432
V. G. Fedoseeva, E. A. Verochkina, L. I. Larina, E. V. Kondrashov, I. B. Rosentsveig, N. V. Vchislo, “Novel capto-dative (Z,E)-2-(alkylthio)alk-2-en-4-ynals: synthesis and heterocyclization”, Mendeleev Commun., 31:6 (2021), 856–858
N. V. Vchislo, V. G. Fedoseeva, V. V. Novokshonov, L. I. Larina, I. B. Rosentsveig, E. A. Verochkina, “Synthesis of new alkoxy/alkylthiovinylated oxazoles using tosylmethyl isocyanide”, Mendeleev Commun., 30:3 (2020), 350–351
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