Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Inga Cikotiene"'
Autor:
Linas Labanauskas, Rita Mazeikaite, Gintaras Urbelis, Olga Gedrimaite, Jurgis Sudzius, Inga Cikotiene
Publikováno v:
ARKIVOC, Vol 2013, Iss 4, Pp 363-376 (2013)
Externí odkaz:
https://doaj.org/article/3ea8e4ec76054f319a63e8964b2ae60e
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1819-1825 (2013)
A N-nitroso moiety can be used for the activation of chloropyrimidines toward a nucleophilic substitution reaction with amines. The subsequent treatment of the obtained products with aq H2SO4 can lead to either N-denitrosation to obtain 4,6-pyrimidin
Externí odkaz:
https://doaj.org/article/2229900082a74e1b921c3ab4d3c0c4d2
Autor:
Jelena Dinić, Miguel X. Fernandes, Milica Pešić, Inga Cikotiene, Ieva Karpaviciene, José M. Padrón, Carla Ríos-Luci
Publikováno v:
Investigational New Drugs
Microtubule targeting agents (MTAs) are extensively used in cancer treatment and many have achieved substantial clinical success. In recent years, targeting microtubules to inhibit cell division has become a widespread pharmaceutical approach for tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d4d4d8fd79e08f6904f7c5c899e84f
https://doi.org/10.1007/s10637-019-00803-6
https://doi.org/10.1007/s10637-019-00803-6
Autor:
Rita Mazeikaite, Gintaras Urbelis, Inga Cikotiene, L. Labanauskas, Jurgis Sudzius, O. Gedrimaite
Publikováno v:
ARKIVOC, Vol 2013, Iss 4, Pp 363-376 (2013)
A convenient synthetic route for preparation of various 4-[4-(1 H-indol-3-yl)butyl]piperazines bearing heterocyclic and aliphatic substituents in position 1 has been developed. During this work some synthetic possibilities of common precursor, 4-[4-(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1a9b687f895f4af32593db75e24bc86
https://doi.org/10.3998/ark.5550190.p008.289
https://doi.org/10.3998/ark.5550190.p008.289
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1819-1825 (2013)
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1819-1825 (2013)
A N-nitroso moiety can be used for the activation of chloropyrimidines toward a nucleophilic substitution reaction with amines. The subsequent treatment of the obtained products with aq H2SO4 can lead to either N-denitrosation to obtain 4,6-pyrimidin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f5f6ca4b8509cc6689af766bd61e2e
https://doi.org/10.3762/bjoc.9.212
https://doi.org/10.3762/bjoc.9.212
Autor:
Algirdas Brukstus, Egidijus Kazlauskas, Inga Cikotiene, Vilma Petrikaite, Daumantas Matulis, Herkus Petrikas
Publikováno v:
Anti-cancer agents in medicinal chemistry. 17(11)
Background: Human Hsp90 chaperone inhibitors are known to be potential anticancer drugs. Previously we have shown a couple of 5-aryl-4-(2,4-dihydroxyphenyl)-1,2,3-thiadiazoles to be promising anticancer agents. Objective: To improve the compounds con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a5b902958c1b275b7e006a6f29cb95
https://pubmed.ncbi.nlm.nih.gov/28270068
https://pubmed.ncbi.nlm.nih.gov/28270068
Autor:
Aurelija Urbanaite, Inga Cikotiene
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3514d8af5d79ec467f429c362611ab0b
https://doi.org/10.1002/chin.201620230
https://doi.org/10.1002/chin.201620230
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dea48d301819fea05a2a1a595861b2f
https://doi.org/10.1002/chin.201612192
https://doi.org/10.1002/chin.201612192
Publikováno v:
Synthesis. 45:448-451
An N-nitroso group was used to activate chloropyrimidines toward nucleophilic substitution by amines. This permitted a simple, one-pot, high-yielding synthesis of pyrimidine-4,6- and -2,4-diamines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::178515c03ad1e963e0342d70e5458df7
https://doi.org/10.1055/s-0032-1317933
https://doi.org/10.1055/s-0032-1317933
Autor:
Inga Cikotiene, Rita Buksnaitiene
Publikováno v:
Advanced Synthesis & Catalysis. 354:2719-2726
Tandem reactions of various acetylenic aldehydes with dimethyl phosphite in basic media were investigated. It was shown that in the case of a non-activated triple bond of the starting materials, the well-known Pudovik reaction followed by a subsequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fea85ef031822128e45e59a0d6f8466
https://doi.org/10.1002/adsc.201200276
https://doi.org/10.1002/adsc.201200276