Synthesis and biological evaluation of indolylglyoxylamide bisphosphonates, antimitotic microtubule-targeting derivatives of indibulin with improved aqueous solubility Научная публикация
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Bioorganic & Medicinal Chemistry Letters
ISSN: 1464-3405 , E-ISSN: 0960-894X |
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| Вых. Данные | Год: 2020, Том: 30, Номер: 23, Номер статьи : 127635, Страниц : DOI: 10.1016/j.bmcl.2020.127635 | ||||||||
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Реферат:
Reactions of 3-tert-butyl-8-methylpyrazolo[5,1-c][1,2,4]triazine with lithium phenyldimethylsilanide and triphenylsilanide in THF media at −85 to −60 °C led to the formation of the silicon C(4)-addition products in high yields. Aromatic 3-tert-butyl-8-methyl-4-(triphenylsilyl)pyrazolo[5,1-c][1,2,4]triazine has been synthesized by oxidation of the corresponding 1,4-dihydro derivative using NBS/Et3N in pentane at −30 to −15 °C. Preferential N(1)-nucleophilic additions of silanides were observed for the sterically hindered 3,4-di-R-8-methylpyrazolo[5,1-c][1,2,4]triazines (R = t-Bu, Ph3Si). Novel C–Si derivatives of 1,2,4-triazines, as well as some other isolated compounds were characterized by IR, 1H, 13C, 29Si NMR, HRMS data and X-ray crystallography.
Библиографическая ссылка:
Brel V.K.
, Artyushin O.I.
, Chuprov-Netochin R.N.
, Leonov S.V.
, Semenova M.N.
, Semenov V.V.
Synthesis and biological evaluation of indolylglyoxylamide bisphosphonates, antimitotic microtubule-targeting derivatives of indibulin with improved aqueous solubility
Bioorganic & Medicinal Chemistry Letters. 2020. V.30. N23. 127635 . DOI: 10.1016/j.bmcl.2020.127635 WOS Scopus OpenAlex
Synthesis and biological evaluation of indolylglyoxylamide bisphosphonates, antimitotic microtubule-targeting derivatives of indibulin with improved aqueous solubility
Bioorganic & Medicinal Chemistry Letters. 2020. V.30. N23. 127635 . DOI: 10.1016/j.bmcl.2020.127635 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000595004500006 |
| Scopus: | 2-s2.0-85094585589 |
| OpenAlex: | W3094353657 |