том 54 издание 8 страницы 1915-1922

Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines

Тип публикацииJournal Article
Дата публикации2005-08-01
scimago Q3
БС2
SJR0.305
CiteScore2.8
Impact factor
ISSN10665285, 15739171
General Chemistry
Краткое описание
Nitro-, nitroso-, and azo-1,2,5-oxadiazoles with 4-R1-5-R2-1,2,3-triazol-1-yl substituents were synthesized by oxidation of amino-(1,2,3-triazol-1-yl)-1,2,5-oxadiazoles (aminotriazolylfurazans). Azido-1,2,5-oxadiazole was prepared by diazotization of amino(triazolyl)furazan followed by treatment of the diazonium salt with sodium azide. Depending on the nature of the substituents and the reagent, triazolylfurazans can undergo destruction to give amino-R-furazans (R = NO2, N3, aminofurazanylazo), the amino group being formed from the triazole ring.
Найдено 
Найдено 

Топ-30

Журналы

1
2
3
4
Russian Chemical Bulletin
4 публикации, 22.22%
New Journal of Chemistry
2 публикации, 11.11%
Mendeleev Communications
1 публикация, 5.56%
Defence Technology
1 публикация, 5.56%
Chinese Chemical Letters
1 публикация, 5.56%
Chemistry - An Asian Journal
1 публикация, 5.56%
ChemInform
1 публикация, 5.56%
Journal of Applied Polymer Science
1 публикация, 5.56%
RSC Advances
1 публикация, 5.56%
Journal of Materials Chemistry A
1 публикация, 5.56%
Organic Letters
1 публикация, 5.56%
1
2
3
4

Издатели

1
2
3
4
Springer Nature
4 публикации, 22.22%
Royal Society of Chemistry (RSC)
4 публикации, 22.22%
Elsevier
3 публикации, 16.67%
Wiley
3 публикации, 16.67%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 5.56%
American Chemical Society (ACS)
1 публикация, 5.56%
1
2
3
4
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
18
Поделиться
Цитировать
ГОСТ |
Цитировать
Batog L. V. et al. Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines // Russian Chemical Bulletin. 2005. Vol. 54. No. 8. pp. 1915-1922.
ГОСТ со всеми авторами (до 50) Скопировать
Batog L. V., Konstantinova L. S., Rozhkov V. Yu. Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines // Russian Chemical Bulletin. 2005. Vol. 54. No. 8. pp. 1915-1922.
RIS |
Цитировать
TY - JOUR
DO - 10.1007/s11172-006-0058-9
UR - http://link.springer.com/10.1007/s11172-006-0058-9
TI - Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines
T2 - Russian Chemical Bulletin
AU - Batog, L V
AU - Konstantinova, L S
AU - Rozhkov, V Yu
PY - 2005
DA - 2005/08/01
PB - Springer Nature
SP - 1915-1922
IS - 8
VL - 54
SN - 1066-5285
SN - 1573-9171
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2005_Batog,
author = {L V Batog and L S Konstantinova and V Yu Rozhkov},
title = {Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines},
journal = {Russian Chemical Bulletin},
year = {2005},
volume = {54},
publisher = {Springer Nature},
month = {aug},
url = {http://link.springer.com/10.1007/s11172-006-0058-9},
number = {8},
pages = {1915--1922},
doi = {10.1007/s11172-006-0058-9}
}
MLA
Цитировать
Batog, L. V., et al. “Synthesis of nitro, nitroso, azo, and azido derivatives of (4-R 1-5-R2-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles by oxidation and diazotization of the corresponding amines.” Russian Chemical Bulletin, vol. 54, no. 8, Aug. 2005, pp. 1915-1922. http://link.springer.com/10.1007/s11172-006-0058-9.