Аннотация:
A novel spirocyclic scaffold of 7'H-spiro[azetidine-3,5'-furo[3,4-d]pyrimidine] chemotype was synthesized in N-Boc-protected form. However, the scaffold was revealed to be unstable to storage when deprotected. The solution was found in the brief removal of the Boc protecting group and rapid acylation of the liberated NH-azetidine with a carboxylic acid imidazolide.
Образец цитирования:
A. Lukin, L. Vinogradova, K. Komarova, M. Krasavin, “Spirocyclic azetidines for drug discovery: Novel Boc-protected 7'H-spiro[azetidine-3,5'-furo[3,4-d ]pyrimidines]”, Mendeleev Commun., 33:3 (2023), 323–324
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc385
https://www.mathnet.ru/rus/mendc/v33/i3/p323
Эта публикация цитируется в следующих 2 статьяx:
Kristina Komarova, Lyubov Vinogradova, Alexey Lukin, Maxim Zhuravlev, Dmitry Deniskin, Mikhail Chudinov, Maxim Gureev, Marine Dogonadze, Natalia Zabolotnykh, Tatiana Vinogradova, Anastasia Lavrova, Petr Yablonskiy, “The Nitrofuran-Warhead-Equipped Spirocyclic Azetidines Show Excellent Activity against Mycobacterium tuberculosis”, Molecules, 29:13 (2024), 3071
Ramón M. Sánchez, Josefa Anaya, Progress in Heterocyclic Chemistry, 36, Progress in Heterocyclic Chemistry (PHC), 2024, 59