Аннотация:
PASE (pot, atom and step economic) synthesis of 1-azolyl-1H-1,2,4-triazole derivatives in up to 91% yield has been accomplished by addition of 5-diazoazoles to ethyl isocyanoacetate.
Образец цитирования:
E. V. Sadchikova, D. L. Alexeeva, V. G. Nenajdenko, “PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate”, Mendeleev Commun., 29:6 (2019), 653–654
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1619
https://www.mathnet.ru/rus/mendc/v29/i6/p653
Эта публикация цитируется в следующих 6 статьяx:
Anton Budeev, Grigory Kantin, Dmitry Dar'in, Mikhail Krasavin, “Diazocarbonyl and Related Compounds in the Synthesis of Azoles”, Molecules, 26:9 (2021), 2530
Nicolai Wippert, Martin Nieger, Claudine Herlan, Nicole Jung, Stefan Bräse, “Synthesis of new pyrazolo[1,2,3]triazines by cyclative cleavage of pyrazolyltriazenes”, Beilstein J. Org. Chem., 17 (2021), 2773
M. A. Prezent, S. V. Baranin, Yu. N. Bubnov, “A convenient synthesis of new (1,2,4-triazolylamino)pyrimidines from cyanamide precursor”, Mendeleev Commun., 30:4 (2020), 500–501
E. V. Sadchikova, D. L. Alexeeva, V. G. Nenajdenko, “Trifluoroacetyl substituted pyrazolotriazines: synthesis and pathways of formation”, Mendeleev Commun., 30:2 (2020), 180–182
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
R. Shevalev, P. A. Zhmurov, D. V. Dar'in, M. Yu. Krasavin, “Taking diazo transfer to water: α-diazo carbonyl compounds from in situ generated mesyl azide”, Mendeleev Commun., 30:3 (2020), 372–373
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