Zobrazeno 1 - 10
of 22
pro vyhledávání: '"L. B. Senyavina"'
Autor:
K. K. Koshoev, S. N. Ananchenko, L. P. Zhebeleva, L. B. Senyavina, A. O. Lailiev, I. V. Torgov
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:1064-1068
1. The reduction of the 17-keto group in ketol (II) with LiAlH4 gives predominantly the 17α-diol (VI), whereas the similar reduction with NaBH4 leads to a mixture of the 17β- and 17α-diols (VII) and (VI) in a 5∶4 ratio. 2. The catalytic hydrogen
Autor:
G. I. Yakovlev, I. I. Chervin, L. B. Senyavina, A. A. Sanasaryan, S. V. Sychev, Yu.A. Ovchinnikov, Vadim T. Ivanov, E. I. Vinogradova, L. A. Fonina
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 23:2225-2232
1. Employing the optical rotation dispersion, IR, and NMR spectroscopy methods, a study was made of the conformation states of some valinomycin analogs with modified side chains, and also of their K+ complexes. 2. A change in the side chains of valin
Publikováno v:
Chemistry of Natural Compounds. 1:310-314
1. A direct comparison of albonoursin with “component 2” isolated from the producing agent of phalamysin (a mutant ofActinomyces noursei) has established their identity. 2. Phenylpyruvic acid and acetone have been identified as products of the ac
Autor:
L. V. Rybin, M. I. Rybinskaya, G. L. Slonimskii, L. B. Senyavina, V. S. Palkov, A. N. Nesmeyanov
Publikováno v:
Bulletin of the Academy of Sciences, USSR Division of Chemical Science. 15:1699-1703
1. Methods were developed for the preparation of cis- and trans-3-benzoylacrylonitriles. 2. The geometric configurations of these isomers were established on the basis of chemical correlations and measurements of the IR and NMR spectra and of dipole
Publikováno v:
Bulletin of the Academy of Sciences, USSR Division of Chemical Science. 15:1541-1545
1. By the Claisen — Schmidt condensation of dehydroacetic acid with substituted benzaldehydes the corresponding substituted 3-cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-ones were obtained. In all cases a mixture of cis- and trans-isomers was formed. I
Autor:
V. D. Vil'chevskaya, Marina I. Struchkova, Yu. N. Sheinker, N. S. Kochetkova, L. B. Senyavina, A. N. Nesmeyanov
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 11:1901-1907
1. In a study of the infrared and ultraviolet spectra of o-carboxybenzoylferrocene and some of its derivatives it was shown that both in the crystals and in solutions these substances exist in the open carboxy form and, within the limits of the sensi
Autor:
E. N. Meshcheryakova, Yu.A. Ovchinnikov, Anatoly I. Miroshnikov, N. N. Uvarova, V. A. Zabrodin, Vladimir F. Bystrov, K. Kh. Khalilulina, S. A. Koz'min, Vadim T. Ivanov, L. B. Senyavina
Publikováno v:
Chemistry of Natural Compounds. 9:353-365
1. A preferred conformation of antamanide in nonpolar solvents has been proposed with the aid of a wide group of physicochemical methods and theoretical analyses. 2. On the basis of spectroscopic results, the hypothesis has been put forward of the ex
Autor:
Vladimir F. Bystrov, Yu.A. Ovchinnikov, L. B. Senyavina, Anatoly I. Miroshnikov, N.D. Abdullaev, E.N. Shepel, E. S. Efremov, Vadim T. Ivanov
Publikováno v:
Biochemical and Biophysical Research Communications. 39:217-225
Conformational study of gramicidin S and N,N′-diacetyl gramicidin S has been carried out by a number of techniques. Optical rotatory dispersion measurements showed both cyclodecapeptides to possess similar conformations in different solvents. Quant
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 11:724-730
1. Absorption bands have been found in the infrared spectra of lactones of cis- and trans-2-oxycyclohexylacetic acid and their functional derivatives, the location of which depends on the configuration at the place where the lactone and cyclohexane r
Autor:
V. V. Shilin, G. A. Kogan, L. B. Senyavina, Yu.A. Ovchinnikov, E. N. Meshcheryakova, Vadim T. Ivanov, E. S. Efremov
Publikováno v:
Tetrahedron Letters. 12:2841-2844