This article is cited in 2 scientific papers (total in 2 papers)
Communications
Reactions of functionally substituted bicyclo[4.2.2]deca-2,4,7,9-tetraenes with m-chloroperbenzoic acid and in vitro evaluation Of Product Cytotoxicity against tumor cells
Abstract:
The oxidation of functionally substituted bicyclo[4.2.2]deca-2,4,7,9-tetraenes with m-chloroperbenzoic acid affords practically valuable 8-oxatricyclo[4.3.2.07,9]undeca-2,4,10-trienes and bicyclo[4.3.1]deca-2,4,8-triene-7,10-diols in yields of 65–72%. The structures of the products were established by advanced spectral methods and X-ray diffraction analysis. The new compounds were screened for in vitro cytotoxicity against Jurkat, K562, U937 and HL60 tumor cell lines.
Citation:
V. A. D'yakonov, G. N. Kadikova, G. F. Gazizullina, I. R. Ramazanov, L. U. Dzhemileva, U. M. Dzhemilev, “Reactions of functionally substituted bicyclo[4.2.2]deca-2,4,7,9-tetraenes with m-chloroperbenzoic acid and in vitro evaluation Of Product Cytotoxicity against tumor cells”, Mendeleev Commun., 29:5 (2019), 517–519
Linking options:
https://www.mathnet.ru/eng/mendc1576
https://www.mathnet.ru/eng/mendc/v29/i5/p517
This publication is cited in the following 2 articles:
Gulnara N. Kadikova, Usein M. Dzhemilev, The 2nd International Electronic Conference on Catalysis Sciences—A Celebration of Catalysts 10th Anniversary, 2021, 2
G. N. Kadikova, V. A. D'yakonov, R. N. Nasretdinov, L. U. Dzhemileva, U. M. Dzhemilev, “Synthesis of new alkynyl containing 9-azabicyclo[4.2.1]nonatrienes from diynes and azepines”, Mendeleev Commun., 30:3 (2020), 318–319
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