Zobrazeno 1 - 10
of 28
pro vyhledávání: '"G. M. Talybov"'
Publikováno v:
Russian Journal of General Chemistry. 92:2989-2992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::068a158ce556a1e561902d6f8db96ed7
https://doi.org/10.1134/s107036322212057x
https://doi.org/10.1134/s107036322212057x
Autor:
G. M. Talybov
Publikováno v:
Russian Journal of General Chemistry. 91:1153-1156
It was shown that propargyl ethers of 2-hydroxyoxiranes in the presence of a silver salt of a molybdenum heteropoly acid as a catalyst leads to the formation of furan derivatives with a yield of up to 62.3% and high regioselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02e2b555817aa4ad57225224a3d7be67
https://doi.org/10.1134/s107036322106027x
https://doi.org/10.1134/s107036322106027x
Publikováno v:
Russian Journal of Organic Chemistry. 56:34-37
Alkoxyhalogenation of dihalostyrenes with allyl or propargyl alcohol and N-bromosuccinimide or crystalline iodine in the presence of clinoptilolite [(NaK)4CaAl6Ci30O72] afforded the corresponding unsaturated β-halo ethers with high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0376ef789ce1b0cd87b1719b6fc469b4
https://doi.org/10.1134/s1070428020010066
https://doi.org/10.1134/s1070428020010066
Autor:
G. M. Talybov
Publikováno v:
Russian Journal of Organic Chemistry. 57:1009-1011
A procedure has been proposed for the synthesis of 2-aryl-5-methyl-1,4-dioxanes by alkoxyiodination of halogen-substituted styrenes with allyl alcohol in the presence of crystalline iodine, (NaK)4CaAl6Si30O72 clinoptilolite, and silicotungstic acid s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e007a16251d59136808315ded1f480e
https://doi.org/10.1134/s1070428021060191
https://doi.org/10.1134/s1070428021060191
Publikováno v:
Russian Journal of Organic Chemistry. 56:552-554
Alkoxyiodination of alkyl allyl ethers with elemental iodine in allyl and propargyl alcohols in the presence of clinoptilolite [(NaK)4CaAl6Si30O72] gave the corresponding alkyl 2-(allyloxy or propargyloxy)-3-iodopropyl ethers in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::090e2df07728adec87ef058ea681469d
https://doi.org/10.1134/s1070428020030318
https://doi.org/10.1134/s1070428020030318
Publikováno v:
Azerbaijan Chemical Journal. :29-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8480cbba2e656d66041ab207789ff4
https://doi.org/10.32737/0005-2531-2019-2-29-34
https://doi.org/10.32737/0005-2531-2019-2-29-34
Publikováno v:
Russian Journal of Organic Chemistry. 55:448-455
Three-component Mannich-type condensation of equimolar amounts of 1-(butylsulfanyl)alkan-2-ols, formaldehyde, and secondary aliphatic and heterocyclic amines at 45–50°C (3–4 h) afforded 65–82% of previously unknown aminomethoxy derivatives whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9c6e1b76cdc75a65bfd4e5e3a0cdbe7
https://doi.org/10.1134/s1070428019040055
https://doi.org/10.1134/s1070428019040055
Publikováno v:
Advances in Intelligent Systems and Computing ISBN: 9783030680039
Synthesis of Compound Esters based on Acid Chloride of Low-Molecular Petroleum Acids of Baku Marine Oil Fields and Chiral Unsaturated Alcohols. The physicochemical properties of the compound naphthenic acid esters are determined, and the possibilitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f0e2ce5755cb71ea53c758f7054d198
https://doi.org/10.1007/978-3-030-68004-6_45
https://doi.org/10.1007/978-3-030-68004-6_45
Autor:
G. M. Talybov
Publikováno v:
Russian Journal of Organic Chemistry. 54:1256-1259
Three-component reaction involving cyclopentane-1,3-dione, substituted benzaldehydes, and chloromethyl propyn(en)yl ethers results in a stereoselective formation of trans-1-aryl-2-{[prop-2-(yn)enyloxy]-methyl}spiro[2,4]hepta-4,7-diones in satisfactor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7dd15c20419c8f07dbafa5b50c103da
https://doi.org/10.1134/s1070428018080225
https://doi.org/10.1134/s1070428018080225
Autor:
G. M. Talybov
Publikováno v:
Russian Journal of Organic Chemistry. 54:393-396
Reactions of cyclic olefins with propargyl and allyl alcohols in the presence of crystalline iodine and a catalytic amount of Ag3PW12O40 afforded in one step trans-1,2-bis[propargyl(allyl)oxy]cycloalkanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9882f44eea568b48370b47deb77766c0
https://doi.org/10.1134/s1070428018030041
https://doi.org/10.1134/s1070428018030041