Zobrazeno 1 - 10
of 28
pro vyhledávání: '"I. P. SKRASTIN'SH"'
Publikováno v:
Pharmaceutical Chemistry Journal. 27:689-692
Publikováno v:
Pharmaceutical Chemistry Journal. 27:624-627
Publikováno v:
ChemInform. 26
Autor:
I. P. Skrastin'sh, L. N. Khokhlova, N. P. Erchak, E. Lukevits, R. O. Vitolinya, G. Ya. Dubur, L. E. Demicheva, V. V. Kastron
Publikováno v:
Pharmaceutical Chemistry Journal. 26:775-778
Highly active cardiovascular preparations are to be found among the 4-aryl derivatives of 1,4-dihydropyridine [i, 3, 5] and 4-furyl-l,4-dihydropyridines exhibiting hypotensive and coronary dilatation activity have been synthesized [2, 6]. There are a
Autor:
G. Ya. Dubur, I. P. Skrastin'sh
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:648-657
Data on the bromination, chlorination, and bromolactonization of 4-aryl-1,4-dihydropyridines are correlated. The reactions of the products of bromination of 4-aryl-1,4-dihydropyridines with various nucleophilic agents (amines and iodide, azide, and t
Autor:
I. P. Skrastin'sh, R. M. Zolotoyabko, A. é. Sausin'sh, V. V. Kastron, G. Ya. Dubur, B. S. Chekavichus
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:989-994
4-Aryl-3,5-dialkoxycarbonyl-2,6-dimethyl-1,4-dihydropyridines are brominated by N-bromosuccinimide in methanol at room temperature at the methyl groups at positions 2 and 6 to form mono-, di-, tri-, and tetrabromo derivatives. When the N-unsubstitute
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:421-424
The action was studied of N-chlorosuccinimide on 2,6-dimethyl-3,5-dialkoxycarbonyl-4-phenyl-1,4-dihydropyridines. 3,4,5,6-Tetrahydropyridines having various degrees of chlorination were obtained according to the ratio between the reagents.
Publikováno v:
Pharmaceutical Chemistry Journal. 29:330-332
Publikováno v:
Pharmaceutical Chemistry Journal. 26:416-418
Autor:
G. Ya. Dubur, R. O. Vitolinya, Agris Adolfovich Kimenis, V. V. Kastron, V. V. Golubeva, I. P. Skrastin'sh
Publikováno v:
Pharmaceutical Chemistry Journal. 25:696-698