Aryne cycloaddition reaction as a facile and mild modification method for design of electrode materials for high-performance symmetric supercapacitor

Autor: Постников, Павел Сергеевич

Covalent modification of graphene-based materials can be considered as one of the most promising methods for tailoring their electrochemical properties and extending their application as electrode materials for supercapacitors. In this contribution,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3626::829b1bb9c08ba4dd794103c5f6d5f4c7
http://earchive.tpu.ru/handle/11683/68314

СИНТЕЗ АЗОТСОДЕРЖАЩИХ ГЕТЕРОЦИКЛИЧЕСКИХ СОЕДИНЕНИЙ НА ОСНОВЕ ПРОИЗВОДНЫХ 9,10-АНТРАХИНОНА

Autor: Tetyana Taras, Oksana Sabadakh, Nikolay P. Matkivsky, Evgeny R. Luchkevich, Vasyl I. Shupeniuk

Publikováno v: Journal of Chemistry and Technologies; Том 28, № 2 (2020): Journal of Chemistry and Technologies; 122-132

A simple glance at FDA databases reveals the structural significance of nitrogen-based heterocycles in the drug design and engineering of pharmaceuticals, with nearly 60 % of unique small-molecule drugs containing a nitrogen heterocycle. Many heteroc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98149c696ac2690aeedc5a0930a577e5
http://chemistry.dnu.dp.ua/article/view/082013

3-Нитро-2-(тригалогенметил)-2H-хромены в реакциях со стабилизированными азометинилидами

Разработаны регио- и стереоселективные методы синтеза трифтор(трихлор)метилзамещенных спиро[хроменопирроли(зи)динов] 2−9, основанные н�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______917::0ec6f5c59044c2a0db0f5b628c766f35
https://hdl.handle.net/10995/96651

Реакции енамино- и азаенаминоиндолов c диенофилами

Работа выполнена при поддержке РФФИ грант 19-03-00720 А.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______917::9b7d5308db9616ef14f12e6c0878c2ca
https://hdl.handle.net/10995/96703

Carbamoylimines of Methyltrifluoropyruvate in the Diels-Alder’s Azareaction with Cyclopentadiene

Autor: Aksinenko, A.Yu., Kalashnikova, I.P., Sokolov, V.B.

Publikováno v: Biomedical Chemistry: Research and Methods; Vol. 1 No. 3 (2018): Special Issue; e00016
Biomedical Chemistry: Research and Methods; Том 1 № 3 (2018): Специальный выпуск; e00016
Biomedical Chemistry: Research and Methods

Carbamoylimines of methyl trifluoropyruvate react with cyclopentadiene with to formation of trifluoromethyl-containing azabicyclo [2.2.1] heptenes and tetrahydrocyclopenta[e][1,3]oxazines. NMR experiments involving DEPT and 1H{19F} determined the str

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=issn26187531::5b9ba3f9ac1b718a39fe5aca9382e419
http://www.bmc-rm.org/index.php/bmcrm/article/view/16