Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Vladimir Akhmetov"'
Autor:
Feifei Xiang, Sven Maisel, Sumit Beniwal, Vladimir Akhmetov, Cordula Ruppenstein, Mirunalini Devarajulu, Andreas Dörr, Olena Papaianina, Andreas Görling, Konstantin Y. Amsharov, Sabine Maier
Publikováno v:
Nature Chemistry. 14:871-876
The [n]cycloparaphenylenes ([n]CPPs)-n para-linked phenylenes that form a closed-loop-have attracted substantial attention due to their unique cyclic structure and highly effective para-conjugation leading to a myriad of fascinating electronic and op
Publikováno v:
Chemistry – A European Journal. 27:17322-17325
Herein, we report a new method for synthesis of extended perylenes and terrylenes. The technique is based on the cascade dehydrative π-extensions (DPEX) of aryl aldehydes, in which stepwise annulations activate previously "dormant" substituents. Two
Publikováno v:
ChemistrySelect. 6:10671-10673
Publikováno v:
Angewandte Chemie (International Ed. in English)
A novel catalyst‐free approach to benzoannulated oxygen‐containing heterocycles from fluorinated oligophenylenes is reported. Unlike existing methods, the presented reaction does not require an oxygen‐containing precursor and relies on an exter
Publikováno v:
Chemical Communications. 57:12325-12328
Caryl–F bond activation has become an important and quickly developing method for construction of carbon-based materials. We report that alumina-mediated C–F bond activation (AmCFA) enables construction of PAHs with zigzag periphery. This method
Autor:
Vladimir Akhmetov, Mikhail Feofanov, Cordula Ruppenstein, Josefine Lange, Dmitry Sharapa, Marjan Krstić, Frank Hampel, Evgeny A. Kataev, Konstantin Amsharov
Publikováno v:
Chemistry – A European Journal. 28
Publikováno v:
Photochemical & Photobiological Sciences. 19:722-725
The synthesis of ten ortho-fused PAHs bearing boronic pinacol ester groups (BPin) is reported. The products are obtained via modification of Mallory photocyclization in 45–99% yields. Among them are examples of highly strained molecules such as [4]
Autor:
Mikhail Feofanov, Andreas Förtsch, Vladimir Akhmetov, Konstantin Amsharov, Sergey I. Troyanov
Publikováno v:
Organic Chemistry Frontiers. 7:1271-1275
An unprecedented [6]helicene's cavity closure indicating the possibility of introducing seven-membered rings via alumina-mediated C–F activation is shown. This finding, in combination with a directed quadruple annulation of fluorinated oligoarylene
Autor:
Vladimir Akhmetov, Mikhail Feofanov, Cordula Ruppenstein, Josefine Lange, Dmitry Sharapa, Marjan Krstić, Frank Hampel, Evgeny A. Kataev, Konstantin Amsharov
Publikováno v:
Chemistry-A European Journal, 28 (31), e202200584
We have discovered a dual (i. e., soft and hard) Lewis acidity of alumina that enables rapid one-pot π-extension through the activation of terminal alkynes followed by C-F activation. The tandem reaction introduces an acenaphthene fragment - an esse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64f1b3d33e4b0e386b9f1dda2ceb1484
https://publikationen.bibliothek.kit.edu/1000146070
https://publikationen.bibliothek.kit.edu/1000146070
Publikováno v:
Green Chemistry, 24 (12), 4761–4765
Pre-treated γ-alumina features reactive centers mimicking electronic interactions of propargyls with transition-metal-based catalysts. The combination of soft π-Lewis acidity and Brønsted basicity allows C-H propargyl activation under mild conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6eb6cbba107a5703b9579b0278d3902
https://publikationen.bibliothek.kit.edu/1000148608/149673513
https://publikationen.bibliothek.kit.edu/1000148608/149673513