Аннотация:
Easily available dimethylmalonoyl peroxide is proposed as a reactive alternative to the widely known spirocyclopropyl analogue for the use in the arene acyloxylation and other oxidative reactions.
Образец цитирования:
M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity”, Mendeleev Commun., 28:5 (2018), 505–507
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1816
https://www.mathnet.ru/rus/mendc/v28/i5/p505
Эта публикация цитируется в следующих 2 статьяx:
O. V. Bityukov, V. A. Vil', N. V. Lukashin, A. G. Cherednichenko, G. I. Nikishin, A. O. Terent'ev, “Solvent-free silica gel mediated decarboxylation of C–O coupling products of β-diketones and β-oxo esters with malonyl peroxides”, Mendeleev Commun., 29:1 (2019), 55–56
V. A. Vil', E. S. Gorlov, O. V. Bityukov, I. B. Krylov, G. I. Nikishin, K. K. Pivnitsky, A. O. Terent'ev, “Oxidative C–O coupling as a new idea in the 'click-like chemistry': malonyl peroxides for the conjugation of two molecules”, Mendeleev Commun., 29:2 (2019), 132–134
Обратная связь: