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New synthesis of tetraoxaspirododecane-diamines and tetraoxazaspirobicycloalkanes

An efficient method for the synthesis of new spiro-tetraoxadodecanediamines and tetraoxazaspirobicycloalkanes has been developed by reactions of primary arylamines with gem-dihydroperoxides and α,ω-dialdehydes (glyoxal, pentanedial) catalyzed by lanthanide catalysts. A potential pathway for formatio...

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Detalles Bibliográficos
Autores principales: Makhmudiyarova, Nataliya N., Shangaraev, Kamil R., Dzhemileva, Lilya U., Tyumkina, Tatyana V., Mescheryakova, Ekaterina S., D'yakonov, Vladimir A., Ibragimov, Askhat G., Dzhemilev, Usein M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072112/
https://www.ncbi.nlm.nih.gov/pubmed/35531552
http://dx.doi.org/10.1039/c9ra06372b
Descripción
Sumario:An efficient method for the synthesis of new spiro-tetraoxadodecanediamines and tetraoxazaspirobicycloalkanes has been developed by reactions of primary arylamines with gem-dihydroperoxides and α,ω-dialdehydes (glyoxal, pentanedial) catalyzed by lanthanide catalysts. A potential pathway for formation of tetraoxaspirododecane-diamines and tetraoxazospirobicycloalkanes has been proposed that involves generation of intermediate tetraoxaspiroalkanediols under the reaction conditions. The structures of the crystalline products have been confirmed by XRD. It was shown that the synthesized tetraoxazaspirobicycloalkanes exhibit high cytotoxic activity against Jurkat, K562, and U937 tumor cultures and Fibroblasts.