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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 6, страницы 697–699 (Mi mendc1295)

Эта публикация цитируется в 6 статьях

Communications

Stereoselective synthesis of the RPSPSPRP isomer of 22-membered P4N2 macrocycles

E. I. Musinaa, T. I. Wittmanna, A. S. Shpaginaa, A. A. Karasika, P. Lӧnneckeb, E. Hey-Hawkinsb

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b Institut für Anorganische Chemie, Universität Leipzig, Leipzig, Germany


Аннотация: Stereoselective synthesis of the first representatives of 1,12-diaza-3,10,14,21-tetraphosphacyclodocosanes was achieved via the Mannich-type condensation of 1,6-bis(phenylphosphino)hexane, formaldehyde and primary amines. Due to covalent self-assembly, individual RPSPSPRP isomer was isolated from a dynamic system containing all possible stereoisomers and a number of by-products.

Ключевые слова: dynamic covalent chemistry, self-assembly, macrocycles, tetrakis-phosphines, 1,12-diaza-3,10,14,21-tetraphosphacyclodocosanes, Mannich-type condensation, stereoselectivity.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.11.002



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