Zobrazeno 1 - 10
of 25
pro vyhledávání: '"M. F. Bundule"'
Autor:
O. N. Akif'ev, L. E. Gnilomedova, M. F. Bundule, V. Ya. Munblit, N. A. Mirzagitova, G. V. Murav'eva
Publikováno v:
Pharmaceutical Chemistry Journal. 29:560-563
Publikováno v:
Pharmaceutical Chemistry Journal. 28:845-849
Crystal and molecular structure of 2-phenyl-3-(n-methyl-P-anisidino)-acetylnaphthoquinone-1,4 (AC-5)
Publikováno v:
Journal of Structural Chemistry. 18:84-87
Publikováno v:
Journal of Structural Chemistry. 26:139-142
Publikováno v:
Journal of Structural Chemistry. 25:309-316
Autor:
F. D. Polyak, A. V. Mishnev, R. Nurdinov, E. E. Liepin'sh, A. V. Eremeev, Ya. Ya. Bleidelis, M. F. Bundule
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:879-883
The reaction of dimethyl 1,4-tetrahydrothiazone-3,5-dicarboxylate with phenyl isocyanate and phenyl isothiocyanate leads to 2,4-dioxo-3-phenyl-9-methoxycarbonyl-7-thia-1,3-diazabicyclo[3.4.O]nonane and its thioxo analog. It is shown that only the tra
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:519-525
It was established by x-ray diffraction analysis that the crystalline title compound exists as a dimer formed by two paired potassium ions bonded to the oxygen atoms of the carboxy group and the coordinated oxygen atoms of the carbonyl groups. The so
Publikováno v:
Journal of Structural Chemistry. 25:769-772
Autor:
A. F. Mishnev, Ya. R. Uldrikis, Ya. Ya. Bleidelis, M. F. Bundule, G. Ya. Dubur, E. A. Bisenieks
Publikováno v:
Chemistry of Heterocyclic Compounds. 23:88-92
Heating 1,1-bis(5,5-dimethyl-1,3-cyclohexanedion-2-yl)acetone with ammonia gave a new heterocyclic compound, namely, 1,4,4,8,8-pentamethyl-2,3,4,5,7,8,9,10-octahydropyrrolo[4,3,2-m,n]acridin-10-one. Analogously, 3,6-dimethyl-9-benzoyl-1,2,3,4,5,6,7,8
Autor:
V. K. Lusis, A. F. Mishnev, G. Ya. Dubur, M. F. Bundule, D. Kh. Mutsenietse, Ya. Ya. Bleidelis
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:1145-1149
The molecular and crystal structure of 2,3a-dimethyl-4-phenyl-3-ethoxycarbony-5-oxo-4a,5-dihydro-4H-indeno[1,2-b]pyridine has been determined, and its reduction and alkaline and acid hydrolysis reactions have been studied.