| Шығарылым |
Атауы |
Файл |
| Том 52, № 5 (2016) |
Oxidation and halogenation of divinyl selenide. first synthesis of divinyl selenoxide |
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Kurkutov E., Potapov V., Amosova S.
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| Том 54, № 7 (2018) |
Oxidation of Adamantane with H2O2–CF3COCF3 · 1.5 H2O in the Presence of VO(acac)2 |
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Kislitsina K., Shchadneva N., Khusnutdinov R.
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| Том 54, № 3 (2018) |
Oxidation of Iodo- and Bromo-Substituted Polymethylbenzenes in the System PbO2–CF3COOH–CH2Cl2 |
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Sandzhieva M., Aryamova E., Sukharzhevskii S., Grinenko E., Vasilyev A.
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| Том 52, № 11 (2016) |
Oxidation of reaction products of p-aryl-С,С-disubstituted nitrones and dimethyl 3-methylenecyclopropane-1,2-dicarboxylate |
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Molchanov A., Tran T., Stepakov A., Kostikov R.
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| Том 55, № 12 (2019) |
Oxidation of Thioamides to Amides with Tetrachloro- and Tetrabromoglycolurils |
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Boudebouz I., Arrous S., Parunov I.
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| Том 52, № 5 (2016) |
Oxidation with CrO3·2Py of levoglucosenone and 1,3-dienes Diels-Alder adducts |
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Biktagirov I., Faizullina L., Salikhov S., Galin F., Safarov M., Valeev F.
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| Том 55, № 6 (2019) |
Oxidative Cyclization of Lithium 4-Ethoxy-1,1,1-trifluoro-4-oxobut-2-en-2-olate |
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Boltacheva N., Slepukhin P., Filyakova V., Charushin V.
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| Том 52, № 4 (2016) |
Oxidative dimerization of 2-chloro-3,3,3-trifluoro- 1-(4-methoxyphenyl)propene in the system PbO2–CF3SO3H |
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Kazakova A., Nenajdenko C., Vasilyev A.
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| Том 53, № 6 (2017) |
Oxidative iodination of N-propargyltriflamide |
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Astakhova V., Ushakov I., Shainyan B.
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| Том 53, № 6 (2017) |
Oxidative transformations of alkyl caryophyllanyl sulfides |
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Gyrdymova Y., Sudarikov D., Rubtsova S., Kutchin A.
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| Том 53, № 7 (2017) |
Oxidative trifluoroacetamidation of (1E,3E)-1,4-diphenylbuta-1,3-diene and 1,1,4,4-tetraphenylbuta-1,3-diene |
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Astakhova V., Moskalik M., Shainyan B.
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| Том 54, № 1 (2018) |
Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones |
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Gornostaev L., Rukovets T., Arnold E., Khalyavina Y., Gatilov Y.
|
| Том 52, № 2 (2016) |
Parquet compounds on the basis of eight- and twelve-membered structure blocks: Quantum-chemical study |
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Gribanova T., Minyaev R., Minkin V.
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| Том 53, № 11 (2017) |
Pd-catalyzed synthesis of 2-alkynyl derivatives of 19β,28-epoxy-18α-olean-1-en-3-one |
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Shakhmaev R., Sunagatullina A., Abdullina E., Zorin V.
|
| Том 55, № 11 (2019) |
Peculiarities of the Reaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-indene-1,3(2H)-dione |
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Gornostaev L., Fominykh O., Lavrikova T., Khalyavina Y., Gatilov Y., Stashina G.
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| Том 52, № 6 (2016) |
Phosphorus-containing Schiff bases and 3,1-benzoxazines |
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Bagautdinova R., Burilov A., Pudovik M., Pudovik E., Dobrynin A.
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| Том 55, № 4 (2019) |
Phosphorylated Glycoconjugates Based on Isosteviol, d-Arabinofuranose, and d-Ribofuranose |
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Sharipova R., Belenok M., Strobykina I., Kataev V.
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| Том 54, № 11 (2018) |
Photocatalytic Synthesis of 1,3-Dioxacyclanes from Diols and Primary Alcohols Effected by a System FeCl3–NaNO2/O2(Air) |
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Makhmutov A.
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| Том 53, № 1 (2017) |
Photochromic benzo[g]indolyl fulgimide with modulated fluorescence |
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Rybalkin V., Zmeeva S., Popova L., Tikhomirova K., Revinskii Y., Dubonosov A., Bren’ V., Minkin V.
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| Том 53, № 3 (2017) |
Photochromic fluorescent indol-3-yl-substituted maleimides |
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Shepelenko E., Makarova N., Podshibyakin V., Tikhomirova K., Dubonosov A., Metelitsa A., Bren V., Minkin V.
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| Том 53, № 4 (2017) |
Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring |
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Chugunova E., Akylbekov N., Samsonov V., Sitnov S., Burilov A.
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| Том 54, № 1 (2018) |
Pincer Receptors for Anions Based on Triazolyl Bile Acids |
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Lukashev N., Erzunov D., Latyshev G., Averin A., Beletskaya I.
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| Том 55, № 10 (2019) |
Plant Coumarins: XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides |
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Zakharov D., Lipeeva A., Gatilov Y., Makarov A., Shults E.
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| Том 52, № 10 (2016) |
Polarity and structure of P(X)-modified (X = O, S) arylcarbamoylmethylphosphine oxides and sulfides |
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Vereshchagina Y., Khanafieva R., Chachkov D., Artyushin O., Sharova E., Ishmaeva E.
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| Том 55, № 5 (2019) |
Polyaromatic Products of Three-Component Coupling of Aryl Halide with Two Molecules of Arylacetylene and Arylboronic Acid under Ligand-Free Catalysis Conditions |
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Yarosh E., Larina E., Lagoda N., Kurokhtina A., Schmidt A.
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| Нәтижелер 1249 - 501/525 |
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