Zobrazeno 1 - 10
of 17
pro vyhledávání: '"E V, Braude"'
Publikováno v:
ChemInform. 25
Publikováno v:
Gigiena truda i professional'nye zabolevaniia. (4)
The article presents results of toxicity and hazard effects studies of alcoxicyandiphenyl CnH2n+ 1OC12H8CN with n = 1-8, octilcyandiphenyl and octildiphenyl. Toxicity parameters were established in animal tests and on isolated mitochondria, and inhib
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:1314-1315
Autor:
E. V. Braude, M. A. Gal'bershtam
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:153-156
The nitration of 5-chloromethylsalicylaldehyde leads to 3-nitro-5-chloromethylsalicylaldehyde, the chlorine atom in which is smoothly replaced by a hydroxy or acetoxy group. The salicylaldehydes obtained condense with 1,3,3-trimethyl-2-methylene-indo
Autor:
M. A. Gal'bershtam, E. V. Braude
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:174-177
5-Nitro-4-phenylsalicylaldehyde, from which the corresponding photochromic indolinespirochromene was obtained, was synthesized. The introduction of a phenyl substituent in the 7 position brings about a substantially smaller change in the longwave ban
Autor:
E. V. Braude, M. A. Gal'bershtam
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:173-179
Styryl-substituted salicylaldehydes were obtained from 5-chloromethylsalicylaldehyde by means of the Wittig reaction, nitration, and several other reactions, and spirochromenes of the indoline series were subsequently synthesized. The possibility of
Autor:
M. A. Gal'bershtam, I. B. Lazarenko, E. V. Braude, N. M. Przhiyalgovskaya, N. P. Samoilova, N. N. Suvorov
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:67-69
The introduction of aryl substituents in the 3′ and 7 positions of the indoline spirochromene molecule gives rise to a certain amount of slowing down of dark decolorization in toluene and dioxane; similar changes in the 5′, 6, and 8 positions do
Autor:
M. A. Gal'bershtam, E. V. Braude
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:823-825
Two photochromic indoline spirochromenes were synthesized. The introduction of a phenyl group into the 6 or 8 position causes a bathochromic shift of the bands in the electronic absorption spectrum of the merocyanine form.
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 16:1790-1792
1. The authors have obtained esters of α-hydroxy acids by alcoholysis of aliphatic α-hydroxynitriles; the yields were 40–75%. 2. A method has been developed for the gas-chromatographic analysis of α-hydroxynitriles and their mixtures with esters
Publikováno v:
Gigiena i sanitariia. (1)