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One-pot synthesis of (1 RS,21 SR)-diethyl 2-[23-amino-22-ethoxycarbonyl-8,11,14-trioxa-25-azatetracyclo[19.3.1.0 2,7.0 15,20]pentacosa-2,4,6,15(20),16,18,22-heptaen-25-yl]but-2-endioate
Tran T.T.V., Le T.A., Truong H.H., Dao T.N., Soldatenkov A.T., Khrustalev V.N.
The title compound, C30 H34 N2 O9 (4), is a product of the Michael reaction of azacrown ether
Complexes of a novel N-(diisopropxythiophosphoryl)thiourea derivative of 1,4,8,11-tetraazacyclotetradecane with Na+, K+ and Cu (PPh3)2 + cations
Safin D., Babashkina M., Sokolov F., Zabirov N., Galezowska J., Kozlowski H.
Azacrown ether
Synthesis by deamination reaction and crystal structure at 120 K of (16 Z,19 E)-18-oxo- N -(pyridin-2-yl)-6,7,9,10-tetra­hydro-18 H -dibenzo[ h, o ][1,4,7]trioxa­cyclo­hexa­decine-17-carboxamide
Wodajo A.T., Tran T.T.V., Truong H.H., Tskhovrebov A.G., Le T.D., Khrustalev V.N., Le T.A.
ether containing the γ-piperidone subunit. The title mol­ecule contains a 16-membered macrocycle
Strategies and methods for the synthesis of pyridinocrownophanes (microreview)
Le A.T., Soldatenkov A.T.
to highlight the most significant recent developments in the synthesis of pyridinofused azacrown ethers, which
Meso-(1S*,21R*)-25-methyl-8,11,14-trioxa- 22,24,25-triazatetracyclo-[19.3.1.02,7.015,20]pentacosa-2, 4,6,15(20),16,18-hexaene-23-thione chloroform monosolvate
Hieu T.H., Anh L.T., Soldatenkov A.T., Kurilkin V.V., Khrustalev V.N.
the azacrown macrocycle and the chloroform solvent molecule. In one of them, the chloroform molecule forms C
Synthesis and molecular structure of bis(benzo)aza-14-crown-4 ethers with 7-azabicyclo[3.3.1]nonane and homologous fragments
Levov A.N., Komarov A.I., Soldatenkov A.T., Avramenko G.V., Soldatova S.A., Khrustalev V.N.
(benzo)-aza-14-crown-4 ethers containing a 7-aza-bicyclo[3.3.1]nonane or its homologous fragment, were obtained
Unexpected formation of dinaphthoaza-17-crown-5 ether containing γ-aminopiperidine subunit
Le A.T., Dao N.T., Truong H.H., Do T.T., Polyakova E.I., Lin'ko I.V., Dorovatovskii P.V., Khrustalev V.N.
(oxy)]di(1-naphthaldehyde) as the podand. The crystal structure of the new azacrown compound was elucidated
Coordination Chemistry of Anticrowns. Interaction of the Perfluorinated Three-Mercury Anticrown (o-C6F4Hg)3 with Azacrowns
Tugashov K.I., Gribanyov D.A., Dolgushin F.M., Smol'Yakov A.F., Peregudov A.S., Klemenkova Z.S., Barakovskaya I.G., Tikhonova I.A., Shur V.B.
) with various azacrowns such as 2,9,16,23-tetra-tert-butylphthalocyanine (TBPC), octaazapentacyclooctacosane
Coordination Chemistry of Anticrowns. Interaction of the Perfluorinated Three-Mercury Anticrown (o-C6F4Hg)3 with Azacrowns
Tugashov K.I., Gribanyov D.A., Dolgushin F.M., Smol'Yakov A.F., Peregudov A.S., Klemenkova Z.S., Barakovskaya I.G., Tikhonova I.A., Shur V.B.
The interaction of the three-mercury anticrown (o-C6F4Hg)3 (1) with various azacrowns such as 2
Синтез и превращения азакраун-эфиров, имеющих азиновые субъединицы
Чыонг Хонг Хиеу
(данные РСА). Truong Hong Hieu (Vietnam) Synthesis and reactions of azacrown ethers with azine subunits A

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