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Неорганические нитрилгалогениды в синтезе галоген-, нитро- и галогеннитропродуктов
Мирошниченко, Ю. Ю., Яркова, А. Г., Передерина, И. А., Тверякова, Е. Н., Голубина, О. А., Анисимова, Е. А., Жолобова, Г. А., Miroshnichenko, Yulia Yu., Yarkova, Anna G., Perederina, Irina A., Tveryakova, Elena N., Golubina, Оlga A., Anisimova, Elena А., Zholobova, Galina A.
Inorganic nitrile halides have been studied theoretically by quantum-chemical approach
ADDITION OF 2-PYRIDYLSELENYL HALIDES TO UNACTIVATED NITRILES
Grishina M.M., Matsulevich Z.V., Borisov A.V., Khrustalev V.N., Tskhovrebov A.G.
ADDITION OF 2-PYRIDYLSELENYL HALIDES TO UNACTIVATED NITRILES
Synthesis of Novel Cationic 1,2,4-Selenadiazoles via Addition of 2-Pyridylselenyl Halides to Unactivated Nitriles
Tskhovrebov A.G.
Synthesis of Novel Cationic 1,2,4-Selenadiazoles via Addition of 2-Pyridylselenyl Halides
Novel supramolecular building blocks based on adducts of 2-pyridylselenyl halides and nitriles: synthesis and self-assembly study
Grudova M.V., Mikhailova I.E., Borisov A.V., Kubasov A.S., Khrustalev V.N., Tskhovrebov A.G.
Novel supramolecular building blocks based on adducts of 2-pyridylselenyl halides and nitriles
2-Pyridylselenenyl versus 2-Pyridyltellurenyl Halides: Symmetrical Chalcogen Bonding in the Solid State and Reactivity towards Nitriles
Buslov I.V., Novikov A.S., Khrustalev V.N., Grudova M.V., Kubasov A.S., Matsulevich Z.V., Borisov A.V., Lukiyanova J.M., Grishina M.M., Kirichuk A.A., Serebryanskaya T.V., Kritchenkov A.S., Tskhovrebov A.G.
. In contrast to 2-pyridylselenenyl halides, the Te congener does not react with nitriles furnishing cyclization
Novel cationic 1,2,4-selenadiazoles: synthesisviaaddition of 2-pyridylselenyl halides to unactivated nitriles, structures and four-center Se⋯N contacts
Khrustalev V.N., Grishina M.M., Matsulevich Z.V., Lukiyanova J.M., Borisova G.N., Osmanov V.K., Novikov A.S., Kirichuk A.A., Borisov A.V., Solari E., Tskhovrebov A.G.
2-Pyridylselenyl halides undergo facile coupling with a triple CN bond of unactivated nitriles
Exploring Supramolecular Assembly Space of Cationic 1,2,4-Selenodiazoles: Effect of the Substituent at the Carbon Atom and Anions
Grudova M.V., Kubasov A.S., Khrustalev V.N., Novikov A.S., Kritchenkov A.S., Nenajdenko V.G., Borisov A.V., Tskhovrebov A.G.
blocks, which can be obtained via coupling between 2-pyridylselenyl halides and nitriles, are virtually
Study of the reactivity of organonickel sigma-complexes towards nitriles
Gafurov Z., Sakhapov I., Babaev V., Dobrynin A., Kurmaz V., Metlushka K., Rizvanov I., Shaikhutdinova G., Sinyashin O., Yakhvarov D.
,4,6-triisopropylphenyl (Tipp), 2,4,6-tricyclohexylphenyl (Tchp), bpy = 2,2´-bipyridine, towards nitriles (acetonitrile
Erratum: Novel cationic 1,2,4-selenadiazoles: synthesisviaaddition of 2-pyridylselenyl halides to unactivated nitriles, structures and four-center Se⋯N contacts (Dalton Transactions (2021) 50 (10689-10691) DOI: 10.1039/D1DT01322J)
Khrustalev V.N., Grishina M.M., Matsulevich Z.V., Lukiyanova J.M., Borisova G.N., Osmanov V.K., Novikov A.S., Kirichuk A.A., Borisov A.V., Solari E., Tskhovrebov A.G.
Erratum: Novel cationic 1,2,4-selenadiazoles: synthesisviaaddition of 2-pyridylselenyl halides
Эволюция реагента йодирования, йоднитрования и оптимизация условий проведения синтеза в рамках зеленой химии
Тверякова, Е. Н., Передерина, И. А., Мирошниченко, Ю. Ю., Голубина, О. А., Юсубов, М. С., Зыкова, М. В., Tveryakova, Elena N., Perederina, Irina A., Miroshnichenko, Yuliya Yu., Golubina, Olga A., Yusubov, Mekhman S., Zykova, Mariya V.
for the formation of potential intermediate particles diiodosilver(I) nitrate and nitrile iodide in solvent

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