Главная Новые поступления Описание Шлюз Z39.50

Базы данных


Публикации Чарушина В.Н. - результаты поиска

Вид поиска

Область поиска
в найденном
 Найдено в других БД:Труды сотрудников Института органического синтеза УрО РАН (18)
Формат представления найденных документов:
полныйинформационныйкраткий
Отсортировать найденные документы по:
авторузаглавиюгоду изданиятипу документа
Поисковый запрос: (<.>A=Mochul`skaya, N. N.$<.>)
Общее количество найденных документов : 18
Показаны документы с 1 по 10
 1-10    11-18 
1.
Инвентарный номер: нет.
   
   T 19


   
    Tandem AN—AN reactions in the synthesis of 1H-pyrrolo[3,2-e]-1,2,4-triazines and products of their oxidative transformations [Electronic resource] / V. N. Charushin, N. N. Mochul`skaya, A. A. Andreiko, M. I. Kodess, I. A. Litvinov, O. G. Sinyashin, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2003. - Vol. 52, № 8. - P1740-1749
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of 3-aryl-1,2,4-triazines with -aminovinyl ketones or ethyl -aminocrotonates in acetic anhydride at room temperature afforded cyclic products of the tandem nucleophilic addition, viz., 3a,4,7,7a-tetrahydro-1H-pyrrolo[3,2-e]-1,2,4-triazines, in good yields. Under oxidative conditions, the latter compounds underwent the pyrrole-ring opening under the action of potassium permanganate to form the corresponding triazinones and were transformed into thriazolyl-substituted pyridines under the action of selenious acid

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2003, 52 (8), 1740.pdf
Найти похожие

2.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and electrochemical properties of fullerene-containing C60-acceptor dyads with fluoronitrobenzene and fluoroquinoxaline moieties as substituents [Electronic resource] / I. P. Romanova, G. G. Yusupova, O. A. Larionova, D. G. Yakhvarov, N. N. Mochul`skaya, L. P. Sidorova, V. V. Zverev, V. N. Charushin, O. G. Sinyashin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2005. - Vol. 54, № 3. - P660-665
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of fullerene C60 with 4-azido-3-fluoro-1-nitrobenzene and 7-azido-6-fluoroquinoxaline afforded earlier unknown cycloadducts (C60-acceptor dyads), in which the electron affinities of the fullerene spheres are comparable with the affinity of nonmodified C60

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2005, 54 (3), 660.pdf
Найти похожие

3.
Инвентарный номер: нет.
   


   
    1,2,4-Triazino[5,6,1-i,j]quinolines: a new type of tricyclic analogs of fluoroquinolones [Electronic resource] / G. N. Lipunova, E. V. Nosova, N. N. Mochul`skaya, A. A. Andreiko, O. M. Chasovskikh, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 4. - P663-667
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of C-aryl-substituted amidrazones and S-methylisothiosemicarbazide with 3-ethoxy-2-polyfluorobenzoylacrylates results in corresponding N-(quinolin-1-yl)amidines that undergo conversion into derivatives of 1,2,4-triazino[5,6,1-i,j]quinoline by heating in acetic anhydride

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (4), 663.pdf
Найти похожие

4.
Инвентарный номер: нет.
   
   A 60


   
    Annelation of the thiazole ring to 1,2,4-triazines by tandem AN—AN or SNH—SNH reactions [Electronic resource] / N. N. Mochul`skaya, A. A. Andreiko, M. I. Kodess, E. B. Vasil'eva, V. I. Filyakova, A. T. Gubaidullin, I. A. Litvinov, O. G. Sinyashin, G. G. Aleksandrov, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 6. - P1279-1289
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of 3-aryl-1,2,4-triazines with aromatic thioamides and 4-arylthiosemicarbazides in acetic anhydride at room temperature afforded cyclic products of the tandem nucleophilic addition reactions, viz., tetrahydrothiazolo[4,5-e]-annelated 1,2,4-triazines, in good yields. The latter underwent aromatization in the presence of potassium permanganate

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (6), 1279.pdf
Найти похожие

5.
Инвентарный номер: нет.
   
   R 30


   
    Reaction of fullerene C60 with 2-azido-4,6-diphenylpyrimidine [Electronic resource] / I. P. Romanova, G. G. Yusupova, D. G. Yakhvarov, O. A. Larionova, N. N. Mochul`skaya, L. P. Sidorova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2003. - Vol. 52, № 10. - P2171-2174
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The first representative of the pyrimidine-substituted [60]fullereno[1,2-b]aziridines was synthesized by the reaction of fullerene C60 with 2-azido-4,6-diphenylpyrimidine. 2-(Azahomo[60]fullereno)-4,6-diphenylpyrimidine was found to be formed as a by-product. The electrochemical properties of the adducts were studied

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2003, 52 (10), 2171.pdf
Найти похожие

6.
Инвентарный номер: нет.
   
   F 70


   
    Fluorine containing quinoline and quinoxaline styryl derivatives: [Electronic resource] / E. V. Nosova, T. V. Trashakhova, V. S. Ustyugov, N. N. Mochul`skaya, M. S. Valova, G. N. Lipunova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 942-947. - Bibliogr. : p. 946-947 (25 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
STYRYLBENZAZINES -- PHOTOLUMINESCENCE -- 6,7-DIFLUOROQUINALDINE
Аннотация: (E)-2-Styryl-substituted 6,7-difluoroquinolines and quinoxalines were synthesized by the condensation of the corresponding 2 methylbenzazines with aromatic aldehydes. Photolumines cence of the synthesized 6,7 difluoro 2 styrylbenzazines was studied

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2011, 60 (5), 942-947.pdf
Найти похожие

7.
Инвентарный номер: нет.
   
   T 19


   
    Tandem A(N)-A(N) reactions in the synthesis of tetrahydrothiazolo[4,5-e][1,2,4]triazines / N. N. Mochul`skaya, P. A. Slepukhin, V. N. Charushin, M. I. Kodess // Mendeleev Communications. - 2016. - Vol. 26, № 5. - С. 375-377. - Bibliogr. : p. 377 (14 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
TRIAZINES -- ACETIC ANHYDRIDE -- SYNTHESIS
Аннотация: Reaction of 3-aryl-1,2,4-triazines with S,N-dinucleophilic N-(het)arylthioureas in acetic anhydride at room temperature affords the cyclization products, tetrahydrothiazolo[4,5-e]-[1,2,4]triazines in good yields. The structure of the heterocyclic system thus formed was confirmed by X-ray diffraction analysis.

\\\\expert2\\NBO\\Mendeleev Communications\\2016, v.26, p. 375-377.pdf
Найти похожие

8.
Инвентарный номер: нет.
   
   M 78


    Mochul`skaya, N. N.
    Three-component cyclization of hydroxylamino-substituted quinoline with reactive methylene compounds and formaldehyde: new method for the synthesis of 7-(isoxazolidin-2-yl)-6-fluoroquinolones [Electronic resource] / N. N. Mochul`skaya, L. P. Sidorova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 11. - P2106-2108
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A one-step procedure was developed for the synthesis of new 6-fluoro-7-(isoxazolidin-2-yl)-4-oxo-1,4-dihydroquinolines. The procedure is based on the 1,3-dipolar cycloaddition of the azomethine oxide and 1,1-disubstituted alkenes, which are generated in situ from 6-fluoro-7-hydroxylamino-4-oxo-1,4-dihydroquinoline-3-carboxylic acid and CH-active compounds (dialkyl malonates, ethyl acetoacetate), respectively, in the presence of formaldehyde at 100—120 °C

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (11), 2106.pdf
Найти похожие

9.
Инвентарный номер: нет.
   
   T 19


   
    Tandem reactions in the synthesis of condensed 1,4-diazines [Text] / V. N. Charushin, P. A. Slepukhin, N. N. Mochul`skaya, L. P. Sidorova, G. L. Rusinov, O. N. Chupakhin // 20-th International Congress of Heterocyclic Chemistry : abstracts. - Palermo, Italy, 2005. - P504
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

Найти похожие

10.
Инвентарный номер: нет.
   
   F 70


   
    Fluoro-containing heterocycles: XIV. Cyclic adducts of 6-fluoro-7-azidoquinoxaline and their transformation products [Electronic resource] / N. N. Mochul`skaya, E. N. Nagibina, Yu. S. Volchenkova, L. P. Sidorova, V. N. Charushin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2005. - Vol. 41, № 11. - P1694-1701. - Библиогр. : с. 1701 (18 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The possibility of a structural modification of quinoxalines through 1,3-dipolar cycloaddition of 7-azido-6-fluoroquinoxaline to norbornenes, enamines of cyclic ketones, and dimethyl acetylenedicarboxylate was demonstarated. The stability of 1,2,3-triazoline adducts was studied and the structure of the products of their molecular rearrangements was established. The cycloadduct of azide with cyclohexanone enamine undergoes azapinacolone rearrangement involving a contruction of the cycloalkane ring by one member affording amidine of cyclopentanecarboxylic acid. The triazoline adduct of the azide with dicyclopentadiene as a result of the rearrangement affords the corresponding aziridinoquinoxaline.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2005, 41 (11), 1694.pdf
Найти похожие

 1-10    11-18 
 

Сиглы отделов ЦНБ УрО РАН


  бр.ф. - Бронированный фонд

  бф - Научно-библиографический отдел

  БХЛ - Фонд художественной литературы

  ИИиА -Фонд исторической литературы в ЦНБ УрО РАН

  ИМЕТ -Отдел ЦНБ в Институте металлургии УрО РАН

  кх - Отдел фондов (книгохранениe)

  МБА - Межбиблиотечный абонемент

  мф - Методический фонд

  ок - Отдел научной каталогизации

  оку - Отдел комплектования и учета

  орф - Обменно-резервный фонд

  пф - Читальный зал деловой и патентной информации

  рк - Фонд редкой книги

  ч/з - Главный читальный зал

  эр - Зал электронных ресурсов

  

Сиглы библиотек институтов и НЦ УрО РАН
© Международная Ассоциация пользователей и разработчиков электронных библиотек и новых информационных технологий
(Ассоциация ЭБНИТ)
Яндекс.Метрика