Аннотация:
Hydroxy-4-methoxytricyclo[7.3.1.02,7]trideca-2,4,6-trien-8-one was synthesized from 1-benzyloxy-4-bromo-2-methoxybenzene in six steps comprising Corey–Chaykovsky epoxidation and Friedel–Crafts intramolecular cyclization. The crystal structure of the benzyl-protected derivative of the target compound was determined by X-ray analysis.
Образец цитирования:
D. V. Shishov, E. V. Nurieva, N. S. Zefirov, A. V. Mamaeva, O. N. Zefirova, “Synthesis of 5-hydroxy-4-methoxytricyclo[7.3.1.02,7]trideca-2,4,6-trien- 8-one – precursor of putative bioisosteric colchicine analogues”, Mendeleev Commun., 24:6 (2014), 370–371
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2586
https://www.mathnet.ru/rus/mendc/v24/i6/p370
Эта публикация цитируется в следующих 4 статьяx:
Jean-François Brière, Stéphane Perrio, Vincent Reboul, Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, 2024
V. V. Burmistrov, V. S. D'yachenko, E. V. Rasskazova, G. M. Butov, “Synthesis of Bicyclic Isocyanates and Bioisosteric 1,3-Disubstituted Ureas as Soluble Epoxide Hydrolase Inhibitors”, Russ J Org Chem, 55:8 (2019), 1166
E. V. Nurieva, N. A. Zefirov, A. V. Mamaeva, Yu. K. Grishin, S. A. Kuznetsov, O. N. Zefirova, “Synthesis of non-steroidal 2-methoxyestradiol mimetics based on the bicyclo[3.3.1]nonane structural motif”, Mendeleev Commun., 27:3 (2017), 240–242
N. A. Zefirov, O. N. Zefirova, “2-Methoxyestradiol and its analogs. Synthesis and structure—antiproliferative activity relationship”, Russ J Org Chem, 51:9 (2015), 1207
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