Zobrazeno 1 - 10
of 371
pro vyhledávání: '"O. A. Erastov"'
Autor:
Yu. Ya. Efremov, Alex Sergey Ionkin, S. N. Ignat'eva, V. M. Nekhoroshkov, O. A. Erastov, B. A. Arbuzov
Publikováno v:
ChemInform. 22
S-Catecholboryl (N,N-dimethylaminomethyl)phenyldithiophosphinate, the first representative of S-diorganylboric derivatives of phosphonous acid was obtained by the reaction of catecholboryl (N,N-dimethylaminomethyl)phenylphosphine with sulfur.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff91138f59c9731498f94ea160c3c292
https://doi.org/10.1002/chin.199123199
https://doi.org/10.1002/chin.199123199
Autor:
N. G. Gazetdinova, O. A. Erastov, A. A. Karasik, O. K. Pozdeev, L. F. Chertanova, Zemfira A. Bredikhina, G. Kh. Gil'manova
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062754d7034e0f28e0ba76867599ad45
https://doi.org/10.1002/chin.199115217
https://doi.org/10.1002/chin.199115217
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f66895936b1dc69b41ec913234dc0fa
https://doi.org/10.1002/chin.199206217
https://doi.org/10.1002/chin.199206217
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:161-165
The reaction between acetone monoalkylhydrazones and aldehydes in the presence of boric acid derivatives has given five-membered boron-nitrogen heterocycles, the stability of which is to a large extent dependent on the substituents in the ring. An x-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00c6d8d46ddc153ecb56bedf674ae7a5
https://doi.org/10.1007/bf00959650
https://doi.org/10.1007/bf00959650
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:165-168
In order to confirm our earlier assumptions with respect to the processes involved in the electrochemical reduction of borylphosphinoethene derivatives, we have analyzed the products of controlled-potential electrolysis. Compounds were isolated and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ad8434fd383550c2bbf418dc3cd1220
https://doi.org/10.1007/bf00959651
https://doi.org/10.1007/bf00959651
Synthesis, structure, and antiviral activity of hydrazinium 5-thia-1,3,2,5-dioxaborataphosphorinanes
Autor:
G. Kh. Gil'manova, N. G. Gazetdinova, O. A. Erastov, L. F. Chertanova, A. A. Karasik, O. K. Pozdeev, Z. A. Bredikhina
Publikováno v:
Pharmaceutical Chemistry Journal. 24:486-489
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27f41e43357200a1dbb18ae817a1868b
https://doi.org/10.1007/bf00764997
https://doi.org/10.1007/bf00764997
Autor:
B. A. Arbuzov, Andrey A. Karasik, S. N. Ignatyeva, G. N. Nikonov, Anna S. Balueva, O. A. Erastov
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. :271-274
Synthetic methods and principal chemical properties of boroxyalkyl derivatives of phosphines are presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00c4bbf5b1282e9df715d43df9bd642e
https://doi.org/10.1080/10426509008038958
https://doi.org/10.1080/10426509008038958
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:688-691
We have established that direct phosphorus-selenium spin-spin coupling constants in cyclic compounds with P=Se exocyclic and P-C endocyclic bonds are found in the range1JPSe=−708 to −859 Hz; in this case, it is greater for the axial orientation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a410d32ea269e08df8a24450978f79c
https://doi.org/10.1007/bf00960327
https://doi.org/10.1007/bf00960327
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:17-20
The intramolecular coordination bonds between phosphoryl-, thio-, and selenophosphoryl groups and boron facilitate the electrochemical reduction of borylphosphinoethene derivatives as compared with their noncyclic analogs. In 1-dibutylboryl-2-dipheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22748d168db6b6ffdb4488a52f55fbeb
https://doi.org/10.1007/bf00962994
https://doi.org/10.1007/bf00962994
Publikováno v:
Bulletin of the Academy of Sciences of The USSR, Division of Chemical Science; 1986, Vol. 35 Issue 1, p160-165, 6p