Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Andrei A. Semioshkin"'
Autor:
Zoya A. Starikova, Igor B. Sivaev, Andrei A. Semioshkin, Vladimir I. Bregadze, Nadezhda Yu. Kulikova, Evgeniya A. Nizhnik, Maxim V. Vichuzhanin
Publikováno v:
Journal of Organometallic Chemistry. 693:519-525
Practical method of synthesis of the 1,4-dioxane derivative of the closo-dodecaborate anion was developed. The cleavage of the dioxonium ring in [B12H11O(CH2CH2)2O]− with acetylenic alcohols gave rise to the preparation of closo-dodecaborate deriva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c6b618aabb106c95526ef3bd8e60ca3
https://doi.org/10.1016/j.jorganchem.2007.11.027
https://doi.org/10.1016/j.jorganchem.2007.11.027
Publikováno v:
Polyhedron. 19:627-632
Direct synthesis of oxonium derivatives of the dodecahydro-closo-dodecaborate anion is described and the reaction mechanism is discussed. Various derivatives of the [B12H12](2-) anion containing hydroxyl, amine, acid, and amino acid functions were pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a195638917a90fb4ecba16c120df7920
https://doi.org/10.1016/s0277-5387(00)00293-x
https://doi.org/10.1016/s0277-5387(00)00293-x
Publikováno v:
Applied Radiation and Isotopes. 67:S91-S93
Cyclic oxonium derivatives of polyhedral boron hydrides have great potential for modification of various types of tumor seeking biomolecules and are very promising starting materials for synthesis of BNCT (boron neutron capture therapy) agents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b197b29be66ad2c5e37edba4dc01216
https://doi.org/10.1016/j.apradiso.2009.03.022
https://doi.org/10.1016/j.apradiso.2009.03.022
Autor:
Andrei A. Semioshkin, V. A. Artyomov, Anatolii M Shestopalov, Vladimir I. Bregadze, G. M. Ptashits, V. P. Litvinov, Vladimir L. Ivanov
Publikováno v:
Tetrahedron. 53:7911-7916
The SN2-type substitution on bromomethyl-o-carborane was never reported earlier. It was found that pyridine-2(1H)-thiones react with bromomethyl-o-carborane in the presence of triethylamine. This reaction leads to the o-carboranylmethylthiopyridines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe1ed907d118d93b4b8bfd5c980cbe4c
https://doi.org/10.1016/s0040-4020(97)00463-8
https://doi.org/10.1016/s0040-4020(97)00463-8
Autor:
Vladimir I. Bregadze, V. P. Litvinov, Vladimir L. Ivanov, Andrei A. Semioshkin, G. M. Ptashits, V. A. Artyomov, Anatolii M Shestopalov
Publikováno v:
ChemInform. 28
The SN2-type substitution on bromomethyl-o-carborane was never reported earlier. It was found that pyridine-2(1H)-thiones react with bromomethyl-o-carborane in the presence of triethylamine. This reaction leads to the o-carboranylmethylthiopyridines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9faf019dc291927d128a80035579480b
https://doi.org/10.1002/chin.199741216
https://doi.org/10.1002/chin.199741216