Abstract:
The FeCl3·6H2O catalyzed Ritter amidation of norbornane dienes with aceto- and propionitriles in the presence of water (145°C, 6h) affords the corresponding amides in yields of 35–87%.
Citation:
R. I. Khusnutdinov, T. M. Egorova, E. S. Meshcheryakova, L. M. Khalilov, U. M. Dzhemilev, “The ferric chloride-catalyzed Ritter amidation of norbornane-type dienes”, Mendeleev Commun., 29:2 (2019), 143–144
Linking options:
https://www.mathnet.ru/eng/mendc1449
https://www.mathnet.ru/eng/mendc/v29/i2/p143
This publication is cited in the following 7 articles:
Fu-Min Zhang, Meng-En Chen, Zhang-Yan Gan, Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, 2024
Meng-En Chen, Xiao-Wei Chen, Yue-Hong Hu, Rui Ye, Jian-Wei Lv, Baosheng Li, Fu-Min Zhang, “Recent advances of Ritter reaction and its synthetic applications”, Org. Chem. Front., 8:16 (2021), 4623
N. V. Yashin, P. O. Markov, K. N. Sedenkova, D. A. Vasilenko, Yu. K. Grishin, T. S. Kuznetsova, E. B. Averina, “Alkyl perchlorates in the Ritter-type reaction. Synthesis of N-alkylamides”, Russ Chem Bull, 69:5 (2020), 980
Ghodsi Mohammadi Ziarani, Fatemeh Soltani Hasankiadeh, Fatemeh Mohajer, “Recent Applications of Ritter Reactions in Organic Syntheses”, ChemistrySelect, 5:45 (2020), 14349
Ravil I. Khusnutdinov, Tatyana M. Egorova, Rishat I. Aminov, Yulia Yu. Mayakova, Ekaterina S. Mescheryakova, “Amidation of deltacyclene and hexacyclic norbornadiene dimers with acetonitrile and water catalyzed by FeCl3·6H2O”, Synthetic Communications, 50:4 (2020), 564
Alexander G. Mikhailovskii, Evgeniya S. Pogorelova, Nataliya N. Pershina, “Synthesis of N-benzylidene- and N-alkylidene(3,3-dialkyl-3,4-dihydroisoquinolin-1(2H)-ylidene)acetohydrazides via the Ritter reaction”, Chem Heterocycl Comp, 56:5 (2020), 562
R. I. Khusnutdinov, A. R. Bayguzina, “New advances in the catalysis of organic reactions by iron compounds”, Russian Chem. Reviews, 89:8 (2020), 824–857
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