| Шығарылым |
Атауы |
Файл |
| Том 55, № 8 (2019) |
Addition of Enolates and Silyl Enol Ethers of Cycloalkanones to Levoglucosenone in the Presence of Lewis Acids |
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Khalilova Y., Faizullina L., Valeev F.
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| Том 53, № 8 (2017) |
Advances in the synthesis of aromatic and heteroaromatic carboxylic acids and their esters |
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Khusnutdinov R., Baiguzina A., Dzhemilev U.
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| Том 55, № 5 (2019) |
Alcoholysis of Binor-S with Alcohols under the Action of Ionic Liquid |
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Aminov R., Khusnutdinov R.
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| Том 52, № 5 (2016) |
Aldehydes of furan series in the synthesis of 1,7-phenanthroline derivatives |
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Kozlov N., Tereshko A.
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| Том 52, № 7 (2016) |
Alkanethiol-promoted stereoselective radical rearrangement of 7-methylidene-6,8-dioxabicyclo[3.2.1]octanes to 2-acetyl-3,4-dihydropyrans |
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Trofimov B., Schmidt E., Bidusenko I., Cherimichkina N.
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| Том 52, № 8 (2016) |
Alkenyl derivatives of 5-nitro-2-pyridone: Synthesis and halocyclization |
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Kalita E., Kim D., Yeltsov O., Shtukina T.
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| Том 54, № 4 (2018) |
Alkoxytelluration of Allylbenzene |
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Musalova M., Musalov M., Udalova S., Khabibulina A., Albanov A., Potapov V., Amosova S.
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| Том 53, № 12 (2017) |
Alkyl 3-nitroacrylates: Synthesis and reactions with cyclohexane-1,3-diones and Meldrum’s acid |
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Pelipko V., Makarenko S., Baichurin R., Berestovitskaya V., Kovalenko K.
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| Том 53, № 6 (2017) |
Alkylation of 1,2,4-triazole-3-thiols with haloalkanoic acid esters |
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Samvelyan M., Ghochikyan T., Grigoryan S., Tamazyan R., Aivazyan A.
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| Том 53, № 8 (2017) |
Alkylation of 2-(hydroxyimino)-5H-[1,3]thiazolo[3,2-a]-pyrimidin-3(2H)-ones |
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Lashmanova E., Larina V., Shiryaev A.
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| Том 53, № 3 (2017) |
Alkylation of 2-methylimidazole with iodomethylsilanes |
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Yarosh N., Zhilitskaya L., Shagun L., Dorofeev I., Larina L.
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| Том 53, № 10 (2017) |
Alkylation of 2-(methylsulfanyl)-6-polyfluoroalkylpyrimidin-4(3H)-ones with haloalkanes |
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Khudina O., Burgart Y., Saloutin V.
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| Том 54, № 8 (2018) |
Alkylation of 2-Sulfanylbenzoxazole with α-Iodoketones in the Absence of Bases |
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Shagun L., Dorofeev I., Zhilitskaya L., Yarosh N., Larina L.
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| Том 55, № 7 (2019) |
Alkylation of 3-tert-Butylpyrimido[4′,5′:3,4]pyrazolo[5,1-c]-[1,2,4]triazine-4,10(1H,9H)-diones and -dithiones |
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Mironovich L., Ivanov S., Daeva E.
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| Том 53, № 2 (2017) |
Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine |
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Omelichkin N., Minyaeva L., Mezheritskii V.
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| Том 54, № 11 (2018) |
Alkylation of 3-Trifluoromethyl-1,2-dihydroquinoxalin-2-one |
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Ivanova A., Burgart Y., Pervova M., Borisevich S., Khursan S., Saloutin V.
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| Том 53, № 7 (2017) |
Alkylation of 4,5-dihydro-1H-imidazole-2-thiol with iodomethylsilanes and -siloxanes |
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Yarosh N., Zhilitskaya L., Shagun L., Dorofeev I., Larina L.
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| Том 55, № 7 (2019) |
Alkylation of 5,5-Substituted N-[4-Methyl-3-phenylfuran-2(5H)-ylidene]-N′-phenylthioureas |
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Avetisyan K., Galstyan L.
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| Том 55, № 6 (2019) |
Alkylation of 6-Polyfluoroalkyl-2-thiouracils with Haloalkanes |
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Khudina O., Ivanova A., Burgart Y., Pervova M., Shatunova T., Borisevich S., Khursan S., Saloutin V.
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| Том 52, № 3 (2016) |
Alkylation of dicarbonyl compounds with 1-bromoadamantane in the presence of metal complex catalysts |
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Khusnutdinov R., Shchadneva N., Khisamova L.
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| Том 53, № 7 (2017) |
Alkylation of methyl 4-chloro-3-oxobutanoate with di- and tribromoalkanes |
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Ismailov V., Ibragimova G., Sadykhova N., Mamedov I., Nagiev F., Yusubov N.
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| Том 52, № 10 (2016) |
Alkylation of methylene-active compounds with halo acetals and hydrolysis of the alkylation products |
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Ismailov V., Yusubov N., Sadykhova N., Gasymov R., Ibragimova G., Mamedov I.
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| Том 55, № 8 (2019) |
Allylation of (R)-2,3-O-Cyclohexylideneglyceraldehyde with Methyl 3-(Bromomethyl)but-3-enoate. Methyl 3-{(2S)-2-[(2R)-1,4-Dioxaspiro[4.5]dec-2-yl]-2-hydroxyethyl}but-3-enoate as a Convenient Universal Building Block for the Synthesis of Key Fragments of Bioactive Compounds |
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Mineeva I.
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| Том 53, № 6 (2017) |
Alternative synthesis of alverine |
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Shakhmaev R., Sunagatullina A., Zorin V.
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| Том 54, № 4 (2018) |
Alternative Synthesis of Isoguvacine and Its N-(2-Aryl-2-hydroxyethyl) Derivatives |
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Abramyants M., Lomov D., Lyashchuk S., Zaporozhets O.
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| Нәтижелер 1249 - 76/100 |
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