Аннотация:
Treatment of 5-, 6- and 7-membered cyclic ketimines bearing alkyl or aryl group with m-chloroperbenzoic acid proceeds as C=N epoxidation and affords bicyclic oxaziridines in good yields, whose subsequent rearrangement gives nitrones.
Образец цитирования:
N. G. Voznesenskaya, O. I. Shmatova, V. G. Nenajdenko, “Transformation of cyclic ketimines to oxaziridines and nitrones”, Mendeleev Commun., 27:1 (2017), 29–30
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1885
https://www.mathnet.ru/rus/mendc/v27/i1/p29
Эта публикация цитируется в следующих 4 статьяx:
Kai Yang, Rui Li, Peiming Gu, “Electrocatalytic conversion of ω-azido carboxylic acids to 1-pyrrolines via a combined process of oxidative decarboxylation and intramolecular Schmidt rearrangement”, Org. Chem. Front., 11:12 (2024), 3391
Yuya Miki, Naohito Tomita, Kazuho Ban, Hironao Sajiki, Yoshinari Sawama, “Synthesis of 1‐Pyrroline by Denitrogenative Ring Expansion of Cyclobutyl Azides under Thermal Conditions”, Adv Synth Catal, 363:14 (2021), 3481
Sundaresan Ravindra, C. P. Irfana Jesin, Arivalagan Shabashini, Ganesh Chandra Nandi, “Recent Advances in the Preparations and Synthetic Applications of Oxaziridines and Diaziridines”, Adv Synth Catal, 363:7 (2021), 1756
O. I. Shmatova, V. G. Nenajdenko, “Synthesis of azacycloalkane-1,2-fused pyrroles via alkylation of cyclic ketimines with α-bromo ketones”, Mendeleev Commun., 28:3 (2018), 270–271
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