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SYNTHESIS AND TRANSFORMATIONS OF METALLACYCLES. 45. CROSS-CYCLOMAGNESIATION OF 1,2-DIENES IN THE SYNTHESIS OF 5Z, 9Z-DIENOIC ACIDS, EFFICIENT INHIBITORS OF HUMAN TOPOISOMERASE I
D’yakonov, V.A., Dzhemileva, L.U., Makarov, A.A., Mulyukova, A.R., Tuktarova, R.A., Islamov, I.I., Dzhemileva, U.M. (2015)
An original method for the synthesis of natural and synthetic 5Z,9Z-dienoic acids with high
CATALYTIC CYCLOMETALLATION IN STEROID CHEMISTRY III1 : SYNTHESIS OF STEROIDAL DERIVATIVES OF 5Z,9Z-DIENOIC ACID AND INVESTIGATION OF ITS HUMAN TOPOISOMERASE I INHIBITORY ACTIVITY
D’yakonov, V.A., Dzhemileva, L.U., Tuktarova, R.A., Makarov, A.A., Islamov, I.I., Mulyukova, A.R., Dzhemilev, U.M. (2015)
Two approaches to stereoselective synthesis of steroid 5Z,9Z-dienoic acids were developed
NOVEL HYBRID MOLECULES ON THE BASIS OF STEROIDS AND (5Z,9Z)-TETRADECA-5,9-DIENOIC ACID: SYNTHESIS, ANTI-CANCER STUDIES AND HUMAN TOPOISOMERASE I INHIBITORY ACTIVITY
D’yakonov, V.A., Dzhemileva, L.U., Tuktarova, R.A., Ishmukhametova, S.R., Yunusbaeva, M.M., Ramazanov, I.R., Dzhemilev, U.M. (2017)
Novel steroid derivatives of 5Z,9Z-dienoic acids were prepared by the DCC
CATALYTIC CYCLOMETALLATION IN STEROID CHEMISTRY III1: SYNTHESIS OF STEROIDAL DERIVATIVES OF 5Z,9Z-DIENOIC ACID AND INVESTIGATION OF ITS HUMAN TOPOISOMERASE I INHIBITORY ACTIVITY
Дьяконов, В.А., Джемилева, Л.У., Туктарова, Р.А., Макаров, А.А., Исламов, И.И., Мулюкова, А.Р., Джемилев, У.М., D’yakonov, Vladimir A., Dzhemileva, Lilya U., Tuktarova, Regina A., Makarov, Aleksey A., Islamov, Ilgiz I., Mulyukova, Alfiya R., Dzhemilev, Usein M. (2015)
Two approaches to stereoselective synthesis of steroid 5Z,9Z-dienoic acids were developed
11-PHENYLUNDECA-5Z,9Z-DIENOIC ACID: STEREOSELECTIVE SYNTHESIS AND DUAL TOPOISOMERASE I/IIΑ INHIBITION
Дьяконов, В.А., Джемилева, Л.У., Макаров, А.А., Мулюкова, А.Р., Хуснутдинова, Э.К., Джемилев, У.М., Толстикова Т. Г., Baev, D.S., D`yakonov, V.A., Dzhemileva, L.U., Makarov, A.A., Mulyukova, A.R., Khusnutdinova, E.K., Dzhemilev, U.M., Tolstikova, Tatiana G. (2015)
(5Z,9Z)-11-Phenylundeca-5,9-dienoic acid was stereoselectively synthesized, based on original cross-cyclomagnesiation
NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA
D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S, Khusnutdinova, Elza K, Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)
unsaturated acids containing a 1Z,5Z-diene group in 61–75 % yields and with[98 % selectivity based on the new
NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA
D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S., Khusnutdinova, Elza K., Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)
unsaturated acids containing a 1Z,5Z-diene group in 61–75 % yields and with >98 % selectivity based on the new
STEREOSELECTIVE SYNTHESIS OF 11-PHENYLUNDECA-5Z,9Z-DIENOIC ACID AND INVESTIGATION OF ITS HUMAN TOPOISOMERASE I AND IIA INHIBITORY ACTIVITY
Дьяконов, В.А., Джемилева, Л.У., Макаров, А.А., Мулюкова, А.Р., Хуснутдинова, Э.К., Джемилев, У.М., Baev, Dmitry S., Tolstikova, Tatiana G., D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulukova, Alfiya R., Khusnutdinova, Elza K., Dzhemilev, Usein M. (2015)
(5Z,9Z)-11-Phenylundeca-5,9-dienoic acid was stereoselectively synthesized, based on original
TOTAL SYNTHESIS OF NEURITOGENIC ALKYNES: LEMBEHYNE B AND KEY INTERMEDIATE OF LEMBEHYNE A
D'yakonov, Vladimir A., Makarov, Aleksey A., Dzhemileva, Lilya U., Andreev, Evgeny N., Dzhemile, Usein M. (2017)
A new Ti-catalyzed cross-cyclomagnesiation of aliphatic and oxygenated 1,2-dienes with Et
THE FIRST TOTAL SYNTHESIS OF THE MARINE ACETYLENIC ALCOHOL, LEMBEHYNE B – A SELECTIVE INDUCER OF EARLY APOPTOSIS IN LEUKEMIA CANCER CELLS
Dzhemileva, L.U., D'yakonov, V.A., Makarov, A.A., Andreev, E.N., Yunusbaeva, M.M., Dzhemilev, U.M. (2017)
alcohol, lembehyne B. The key stage of the process uses new cross-cyclomagnesiation reaction of aliphatic

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