Zobrazeno 1 - 10
of 15
pro vyhledávání: '"S. G. Bandaev"'
Publikováno v:
Russian Journal of Organic Chemistry. 57:1656-1661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7e15907cdaafa1bf6444e224fe1c1db
https://doi.org/10.1134/s1070428021100146
https://doi.org/10.1134/s1070428021100146
Autor:
E. V. Trofimova, S. G. Bandaev, S. S. Mochalov, T. E. Gulov, A. N. Fedotov, Nikolay S. Zefirov
Publikováno v:
Russian Journal of Organic Chemistry. 49:1534-1541
Sovomercuration adducts of 2-nitrobenzyl-, 2-nitro-4,5-(ethylenedioxy)benzyl-, and 4,5-dimethoxy-2-nitrobenzylcyclopropanes were synthesized. The adducts reacted with sulfuric, fluorosulfonic, or chlorosulfonic acid to give 3-(2-chloromercurio)ethyl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04b53b0a64b2160140e9d1de5b5be539
https://doi.org/10.1134/s1070428013100217
https://doi.org/10.1134/s1070428013100217
Publikováno v:
Moscow University Chemistry Bulletin. 67:122-126
The reaction of benzylcyclopropanes to mercury (II) acetate in formic acid proceeds regioselectively and results in high yields of organomercuric compounds. It was shown that the formyloxy group in the homobenzyl position of 4-chloromercury-substitut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae58e142f60560cb11403bac79b1ff58
https://doi.org/10.3103/s0027131412030091
https://doi.org/10.3103/s0027131412030091
Publikováno v:
Moscow University Chemistry Bulletin. 70:40-42
A method is proposed for synthesizing the dimer of 1,4-benzodiazepin-2-one with a cyclobutane-1,2-diyl linker. In this dimer, C5 atoms of monomeric heterocycles are bound to vicinal carbon of cyclobutane.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36d64920d7f00dee0add5681e39a20ae
https://doi.org/10.3103/s0027131415010034
https://doi.org/10.3103/s0027131415010034
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fb0e32b3d3d9adb72779e7fee350e82
https://doi.org/10.1002/chin.199914174
https://doi.org/10.1002/chin.199914174
Publikováno v:
Russian Chemical Bulletin. 47:2300-2301
2-Ethoxycarbonylmethyl-7-methyl-1,3,4-thiadiazolo[3,2-a]pyrimidin-5(5H)-one containing the active methylene group reacts easily with carbon disulfide and phenyl isothiocyanate in the presence of sodium hydride. Further alkylation of the reaction prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c44603f1c830b6ad02287f56b5aba375
https://doi.org/10.1007/bf02494301
https://doi.org/10.1007/bf02494301
Publikováno v:
Journal of Organometallic Chemistry. 99:213-222
Mercuration of trans-1-phenyl-2-cyclohexylcyclopropane and stereoisomeric 1,2-di- and 1,2,3-triphenylcyclopropanes has been studied. An increase in the number of substituents in the cyclopropane ring leads to an increase in the stability of the ring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c64868cfd34766e8d349670a961d2fdd
https://doi.org/10.1016/s0022-328x(00)88450-8
https://doi.org/10.1016/s0022-328x(00)88450-8
Publikováno v:
Journal für Praktische Chemie. 322:643-648
Stereochemistry of Ring Opening of trans-1,2-Diphenylcyclopropanes by Mercury(II) salts Reaction of trans-1,2-diphenylcyclopropanes 1 and 2 with mercuric salts yields diastereomeric 1,2-diphenylpropanole derivatives. The ratio of erythro and threo di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5535f13e52aed6324a2ced6c02a99e64
https://doi.org/10.1002/prac.19803220416
https://doi.org/10.1002/prac.19803220416
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa9825f345da8487c73553215390a0f8
https://doi.org/10.1002/chin.197605275
https://doi.org/10.1002/chin.197605275
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b2288a8c34af60888bd55f535fdddf
https://doi.org/10.1002/chin.198030217
https://doi.org/10.1002/chin.198030217