Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Natalia Soldatova"'
Autor:
Natalia Soldatova, Pavel Postnikov, Olga Kukurina, Viktor V. Zhdankin, Akira Yoshimura, Thomas Wirth, Mekhman S. Yusubov
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 849-855 (2018)
A facile synthesis of diaryliodonium salts utilizing Oxone as versatile and cheap oxidant has been developed. This method shows wide applicability and can be used for the preparation of iodonium salts containing electron-donating or electron-withdraw
Externí odkaz:
https://doaj.org/article/54d18752434048ea8ea4a6e3b46ed962
Autor:
Amirbek Radzhabov, Natalia Soldatova, Daniil Ivanov, Mekhman Yusubov, Vadim Kukushkin, Pavel Postnikov
The rational search for the efficient protocols for atom-efficient arylation utilizing iodonium salts is the genuine need for the sustainability and green chemistry. We developed a novel approach toward metal-free diarylation of selenocyanate using t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c4296ab9d79c81866e3a8c90a4c901f
https://doi.org/10.26434/chemrxiv-2023-zb8fd
https://doi.org/10.26434/chemrxiv-2023-zb8fd
Autor:
Irina Fedorova, Natalia Soldatova, Daniil Ivanov, Ksenia Nikiforova, Irina Aliyarova, Mekhman Yusubov, Peter Tolstoy, Rosa Gomila, Antonio Frontera, Vadim Kukushkin, Pavel Postnikov, Giuseppe Resnati
The simultaneous binding of a molecular entity through two interactions is a frequently pursued recognition mode due to the advantages it offers in securing molecular self-assembly. Here we report how the planarity of the benzothienoiodolium (BTI) ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17332bb5d55ef9189c38bf1f812826c
https://doi.org/10.26434/chemrxiv-2022-1fb3b
https://doi.org/10.26434/chemrxiv-2022-1fb3b
Autor:
Ekaterina Podrezova, Alina Okhina, Artem Rogachev, Sergey Baykov, Andreas Kirschning, Mekhman Yusubov, Natalia Soldatova, Pavel Postnikov
The arylation of azaheterocycles can be considered as one of the most important processes for the preparation of various biologically active compounds. In the present work, we describe a method for the copper-catalyzed N-arylation of hindered oxazoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b1a9a2507701b85b40b386c26b60cda
https://doi.org/10.26434/chemrxiv-2022-xnmf7
https://doi.org/10.26434/chemrxiv-2022-xnmf7
Autor:
Natalia Soldatova, Artem Semenov, Kirill Geyl, Sergey Baykov, Anton Shetnev, Anna Konstantinova, Mikhail Korsakov, Mekhman Yusubov, Pavel Postnikov
The direct N-arylation of cyclic amides can be considered a pivotal issue for modern organic chemistry. Here, we report the method for copper-catalyzed N-arylation of diverse oxadiazolones by diaryliodonium salts in mild conditions in high yields (up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e21012af50bac1d97a30627ddd1af3
https://doi.org/10.26434/chemrxiv.14368985
https://doi.org/10.26434/chemrxiv.14368985
Publikováno v:
"Smart Technologies" for Society, State and Economy ISBN: 9783030591250
The article is devoted to the study of marketing concepts related to innovative products. Modern marketing theory concerning innovative startups is underdeveloped. There is no basic marketing framework without which startupers can hardly understand w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9eeac3a24f39d826efbe9cb1db55163
https://doi.org/10.1007/978-3-030-59126-7_184
https://doi.org/10.1007/978-3-030-59126-7_184
Autor:
Dmitry Ryabukhin, Alexey Turdakov, Natalia Soldatova, Mikhail Kompanets, Alexander Ivanov, Irina Boyarskaya, Aleksander Vasilyev
Interaction of 2-carbonyl and 2-hydroxy(or methoxy)alkyl benzimidazoles with arenes in the Brønsted superacid TfOH resulted in the formation of the corresponding Friedel-Crafts reaction products, 2-diarylmethyl and 2-arylmethyl substituted benzimida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b488a7ba980ecc3b4e9a01f2ef357b42
https://doi.org/10.3762/bxiv.2019.6.v1
https://doi.org/10.3762/bxiv.2019.6.v1