Zobrazeno 1 - 10
of 32
pro vyhledávání: '"A. V. Lipeeva"'
Autor:
Artemii A. Ivanov, Egor A. Ukladov, Stepan A. Kremis, Sodbo Z. Sharapov, Sergey I. Baiborodin, Alla V. Lipeeva, Elvira E. Shults, Tatiana S. Golubeva
Publikováno v:
Protoplasma. 259:1321-1330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1d7113f0a64497a03ed69989c210c87
https://doi.org/10.1007/s00709-022-01739-0
https://doi.org/10.1007/s00709-022-01739-0
Autor:
Alla V. Lipeeva, Elvira E. Shults, Makhmut M. Shakirov, Mikhail A. Pokrovsky, Andrey G. Pokrovsky
Publikováno v:
Molecules, Vol 19, Iss 6, Pp 7881-7900 (2014)
A series of new analogs of combretastatin A-4 (CA-4, 1) with the A or B-ring replaced by a 3-oxo-2,3-dihydrofurocoumarin or a furocoumarin residue have been designed and synthesized by employing a cross-coupling approach. All the compounds were evalu
Externí odkaz:
https://doaj.org/article/736f4c3ab04d4fdcbb5142184ce2edef
Autor:
Alla V. Lipeeva, Danila O. Zakharov, Liubov G. Burova, Tatyana S. Frolova, Dmitry S. Baev, Ilia V. Shirokikh, Alexander N. Evstropov, Olga I. Sinitsyna, Tatyana G. Tolsikova, Elvira E. Shults
Publikováno v:
Molecules, Vol 24, Iss 11, p 2126 (2019)
Synthesis of 1,2,3-triazole-substituted coumarins and also 1,2,3-triazolyl or 1,2,3-triazolylalk-1-inyl-linked coumarin-2,3-furocoumarin hybrids was performed by employing the cross-coupling and copper catalyzed azide-alkyne cycloaddition reaction ap
Externí odkaz:
https://doaj.org/article/b3ec096e033f4bf7b50bb3586caaef2f
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:125-132
In the reaction of coumarin peuruthenicin with α,ω-dibromoalkanes, the corresponding 7-(ω-bromoalkyloxy)coumarins have been synthesized. The interaction of the resulting compounds with sodium azide has yielded 7-(ω-azidoalkyl)-substituted peuruth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75d90bc619b8ddf9feadd50e5ed457c2
https://doi.org/10.1134/s1068162020010161
https://doi.org/10.1134/s1068162020010161
Autor:
Artemii A, Ivanov, Egor A, Ukladov, Stepan A, Kremis, Sodbo Z, Sharapov, Sergey I, Baiborodin, Alla V, Lipeeva, Elvira E, Shults, Tatiana S, Golubeva
Publikováno v:
Protoplasma. 259(5)
High biological activity of natural furocoumarins is often linked to a series of adverse side effects, e.g., genotoxicity. This makes it desirable to develop semi-synthetic derivatives with reduced negative activity while retaining or even enhancing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::59d71013d5095b313141b5f957fcc72e
https://pubmed.ncbi.nlm.nih.gov/35080665
https://pubmed.ncbi.nlm.nih.gov/35080665
Publikováno v:
Russian Journal of Organic Chemistry. 55:1518-1526
Umbelliferone-6-carbonyl chloride reacted with amines and α-, β-, and ω-amino acid methyl esters to afford the corresponding N-substituted 7-hydroxy-2-oxo-2H-chromene-6-carboxamides. The reaction of umbelliferone-6-carbonyl chloride with glycine g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc697f383834f10a0bf5cc2014c0539d
https://doi.org/10.1134/s1070428019100099
https://doi.org/10.1134/s1070428019100099
Autor:
M. A. Pokrovskii, A. G. Pokrovskii, Elvira E. Shults, Yurii V. Gatilov, Danila O. Zakharov, A. V. Lipeeva
Publikováno v:
ChemistrySelect. 4:10197-10201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24219ae8bde55eaeac06e6c660a25845
https://doi.org/10.1002/slct.201901377
https://doi.org/10.1002/slct.201901377
Publikováno v:
Synthetic Communications. 49:3301-3310
Palladium-catalyzed synthesis of 2H-pyrano[2,3-g]isoquinolinones have been described from easily accessible precursor 6-cyanoumbelliferone triflate via sequential of Sonogashira coupling an...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ab1dc891591785b2877e9ba03b939e8
https://doi.org/10.1080/00397911.2019.1661480
https://doi.org/10.1080/00397911.2019.1661480
Publikováno v:
Current Bioactive Compounds. 15:71-82
Background: Coumarin and modified nitrogen heterocyclic nuclei show biological activity. Combining these into a hybrid molecule could lead to new pharmacological agents. A series of hybrid compounds combining coumarin and piperidine, piperazine, puri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::323f8fa6c53f51faf536a862e9b9eff6
https://doi.org/10.2174/1573407213666171030152601
https://doi.org/10.2174/1573407213666171030152601
Autor:
Elvira E. Shults, A. V. Lipeeva
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:1302-1309
7-Alkynyl-substituted coumarins were synthesized by a Sonogashira reaction of 6-substituted 7-(trifluoromethylsulfonyloxy)coumarins with terminal acetylenes. The reaction of 7-ethynyl-substituted coumarins with azidobenzoic acids in the presence of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::784d1ceb61583420e64bbe58390901b8
https://doi.org/10.1007/s10593-018-2210-5
https://doi.org/10.1007/s10593-018-2210-5