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Публикации в базе данных Math-Net.Ru
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Формирование перспективных для электронно-лучевой и экстремально-ультрафиолетовой нанолитографии тонкопленочных резистивных материалов на основе оловоорганических оксокластеров
ЖТФ, 96:2 (2026), 383–394
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Moving of the tetramethylbutanediyl substituent over the catecholcarbaldehyde core
Mendeleev Commun., 36:1 (2026), 117–119
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Halogen-substituted salicylhydroximate copper(II) metallacrowns: from synthesis and structures to novel applications
Mendeleev Commun., 33:1 (2023), 37–40
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New tri-tert-alkyl substituted o-quinones of tetraline family
Mendeleev Commun., 32:4 (2022), 540–542
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Synthesis and structure of sterically hindered o-benzoquinone carboxylic acid
Mendeleev Commun., 31:2 (2021), 268–270
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Utilizing o-quinone methide chemistry: synthesis of sterically hindered acridin-4-ols
Mendeleev Commun., 31:2 (2021), 262–264
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Trans-etherification of catechol-type benzylic ether with diols as a route to new sterically hindered bis-catechols
Mendeleev Commun., 29:1 (2019), 91–93
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New sterically hindered bis-catechol, bis-o-quinone and its bis-triphenylantimony(v) bis-catecholate. 3,5-Di-tert-butyl-6-methoxymethylcatechol as alkylating agent
Mendeleev Commun., 28:1 (2018), 76–78
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New sterically-hindered catechols/o-benzoquinones. Reduction of 4,6-di-tert-butyl-2,3-dihydroxybenzaldehyde
Mendeleev Commun., 26:6 (2016), 552–554
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New bis-o-quinone with azine spacer and its cyclization into indazolo[2,1-a]indazole system
Mendeleev Commun., 25:4 (2015), 312–314
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