Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Alexander A. Kislukhin"'
Autor:
Alexander S. Arseniev, Dmitrii I. Moskvin, Ilia V. Yampolsky, Yulii Aleksandrovich Labas, Mikhail S. Baranov, Konstantin S. Mineev, Alexander A. Kislukhin, Pavel E. Ivashkin, Zinaida M. Kaskova, Roman Gritсenko, Svetlana G. Postikova
Publikováno v:
Synlett. 28:583-588
Panal is a natural bicyclic cadalane-type sesquiterpenoid with an unusual combination of stereocenters. It was isolated in 1988 as an alleged biosynthetic precursor of luciferin (a light-emitting molecule) in a bioluminescent fungus Panellus stipticu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75362395b8297c74d1e1969cc6a43d2a
https://doi.org/10.1055/s-0036-1588104
https://doi.org/10.1055/s-0036-1588104
Paramagnetic fluorinated nanoemulsions for sensitive cellular fluorine-19 magnetic resonance imaging
Autor:
Hongyan Xu, Stephen R. Adams, Eric T. Ahrens, Alexander A. Kislukhin, Roger Y. Tsien, Kazim H. Narsinh
Publikováno v:
Nature materials
Fluorine-19 magnetic resonance imaging ((19)F MRI) probes enable quantitative in vivo detection of cell therapies and inflammatory cells. Here, we describe the formulation of perfluorocarbon-based nanoemulsions with improved sensitivity for cellular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f2976b429537a56f431dfbce77cde93
https://doi.org/10.1038/nmat4585
https://doi.org/10.1038/nmat4585
Autor:
M. G. Finn, Clinton S. Potter, Alexandra Castillejos, Bridget Carragher, Marisa L. Hovlid, Cody J. Higginson, Alexander A. Kislukhin, Melody G. Campbell, Florian Manzenrieder, Neil R. Voss, Jason D. Fiedler
Publikováno v:
Biomacromolecules. 13:2339-2348
The single-coat protein (CP) of bacteriophage Qβ self-assembles into T = 3 icosahedral virus-like particles (VLPs), of interest for a wide range of applications. These VLPs are very stable, but identification of the specific molecular determinants o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37728c9451f1d502d06bec2f463e0264
https://doi.org/10.1021/bm300590x
https://doi.org/10.1021/bm300590x
Publikováno v:
Organic Letters. 13:1832-1835
Both inter- and intramolecular degradation pathways were identified for the aqueous phase deactivation of oxanorbornadiene (OND) electrophiles, and propargylic OND esters were found to undergo facile intramolecular [2 + 2 + 2] homo-Diels-Alder cycloa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3566d94e55ff1c66b01b82a094e6117a
https://doi.org/10.1021/ol103153f
https://doi.org/10.1021/ol103153f
Publikováno v:
Journal of the American Chemical Society. 131:9986-9994
Thiol alkylation is a powerful technique for the labeling of proteins. We report a new class of highly reactive, selective, and fluorogenic probes for thiols in aqueous solution at neutral pH, based on the 7-oxanorbornadiene (OND) framework. The male
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed4770a19f711c76922349c626ff98d8
https://doi.org/10.1021/ja809345d
https://doi.org/10.1021/ja809345d
Autor:
Konstantin A. Lyssenko, T. V. Skrupskaya, A. V. Shevtsov, Alexander A. Kislukhin, Nina N. Makhova, V. Yu. Petukhova
Publikováno v:
Russian Chemical Bulletin. 57:56-62
Complexes of αω-bis(3,3-dialkyldiaziridin-1-yl)alkanes and their bis(2-arylcarbamoyl) derivatives with Cd2+ and Ni2+ salts were synthesized. The X-ray diffraction study showed that only one molecule of the starting bis-diaziridine is involved in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::078da1173c89b9ca5a6a00347ff1ccc6
https://doi.org/10.1007/s11172-008-0008-9
https://doi.org/10.1007/s11172-008-0008-9
Autor:
Vladimir V. Kuznetsov, Yu. A. Strelenko, Konstantin A. Lyssenko, Alexander A. Kislukhin, Nina N. Makhova, Vera Yu. Petukhova, A. V. Shevtsov
Publikováno v:
Journal of Heterocyclic Chemistry. 43:881-888
The reactions of 1,5-diazabicyclo[3.1.0]hexanes 8 with arylketenes 1 have been studied in different conditions. The 1-(arylacethyl)pyrazolidines 11 were obtained at −30 °C in ether and at 20 °C in benzene instead of the expected bicyclic systems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be10dcb840152bee1fef719c36ac278e
https://doi.org/10.1002/jhet.5570430411
https://doi.org/10.1002/jhet.5570430411
Autor:
Anastasia L. Patterson, Alexander A. Kislukhin, Bryan J. Visser, David A. Vosburg, Mary D. May
Publikováno v:
Journal of chemical education. 90(12)
A green organic laboratory experiment was developed in which students synthesize a sensor for thiols using a microscale, solventless Diels–Alder reaction at room temperature or 37 °C. The molecular probe is easily purified by column chromatography
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e410d73686fbc098f1ba932f9987aef
https://pubmed.ncbi.nlm.nih.gov/24415795
https://pubmed.ncbi.nlm.nih.gov/24415795
Autor:
Vladimir V. Kuznetsov, Konstantin A. Lyssenko, A. V. Shevtsov, Vera Yu. Petukhova, V. A. Maslennikov, Alexander A. Kislukhin, Nina N. Makhova, Alexandra O. Borissova
Publikováno v:
Mendeleev Communications. 17:119-121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f3470bb96ac213c8b8b84890924e02e
https://doi.org/10.1016/j.mencom.2007.03.023
https://doi.org/10.1016/j.mencom.2007.03.023
Copper-catalyzed azide–alkyne cycloaddition (CuAAC) has found numerous applications in a variety of fields. We report here only modest differences in the reactivity of various classes of terminal alkynes under typical bioconjugative and preparative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1dceedf9a44fd5ae0fca8e29f9569bc
https://europepmc.org/articles/PMC4170714/
https://europepmc.org/articles/PMC4170714/
