Rhodium‐Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with Benzothiadiazol‐Containing Acetylenes: Access to Isoquinoline‐Bridged Donor‐Acceptor Luminophores
Тип публикации: Journal Article
Дата публикации: 2022-04-03
scimago Q2
wos Q2
БС2
SJR: 0.558
CiteScore: 4.3
Impact factor: 2.7
ISSN: 1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Краткое описание
An efficient strategy for the preparation of a novel series of benzothiadiazole‐containing isoquinoline‐bridged D‐A compounds based on Cp*Rh(III)‐catalyzed redox‐neutral annulation ofN‐(pivaloyloxy)‐benzamides with 4‐ethynyl‐7‐(p‐methoxyphenyl)‐2,1,3‐benzothiadiazole as a key step followed by the installation of donor units, such as diphenylamine, carbazole, and dihydrodibenzoazepine, by aromatization and Suzuki coupling reactions, has been developed. An initial photophysical, electrochemical and DFT investigations of the selected products have been performed.
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Топ-30
Журналы
|
1
2
|
|
|
Asian Journal of Organic Chemistry
2 публикации, 25%
|
|
|
Organic Letters
1 публикация, 12.5%
|
|
|
Progress in Heterocyclic Chemistry
1 публикация, 12.5%
|
|
|
Mendeleev Communications
1 публикация, 12.5%
|
|
|
Russian Chemical Reviews
1 публикация, 12.5%
|
|
|
Molecules
1 публикация, 12.5%
|
|
|
Organic and Biomolecular Chemistry
1 публикация, 12.5%
|
|
|
1
2
|
Издатели
|
1
2
|
|
|
Wiley
2 публикации, 25%
|
|
|
American Chemical Society (ACS)
1 публикация, 12.5%
|
|
|
Elsevier
1 публикация, 12.5%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 12.5%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 12.5%
|
|
|
MDPI
1 публикация, 12.5%
|
|
|
Royal Society of Chemistry (RSC)
1 публикация, 12.5%
|
|
|
1
2
|
- 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
8
Всего цитирований:
8
Цитирований c 2025:
1
(12.5%)
Цитировать
ГОСТ |
RIS |
BibTex
Цитировать
ГОСТ
Скопировать
Gribanov P. S. et al. Rhodium‐Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with Benzothiadiazol‐Containing Acetylenes: Access to Isoquinoline‐Bridged Donor‐Acceptor Luminophores // European Journal of Organic Chemistry. 2022. Vol. 2022. No. 13.
ГОСТ со всеми авторами (до 50)
Скопировать
Gribanov P. S., Vorobyeva D. V., Tokarev S. D., Petropavlovskikh D. A., Loginov D. A., Nefedov S. E., Dolgushin F. M., Osipov S. N. Rhodium‐Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with Benzothiadiazol‐Containing Acetylenes: Access to Isoquinoline‐Bridged Donor‐Acceptor Luminophores // European Journal of Organic Chemistry. 2022. Vol. 2022. No. 13.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1002/ejoc.202101572
UR - https://doi.org/10.1002/ejoc.202101572
TI - Rhodium‐Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with Benzothiadiazol‐Containing Acetylenes: Access to Isoquinoline‐Bridged Donor‐Acceptor Luminophores
T2 - European Journal of Organic Chemistry
AU - Gribanov, Pavel S
AU - Vorobyeva, Daria V
AU - Tokarev, Sergey D
AU - Petropavlovskikh, Dmitry A
AU - Loginov, Dmitry A
AU - Nefedov, Sergey E.
AU - Dolgushin, Fedor M.
AU - Osipov, Sergey N.
PY - 2022
DA - 2022/04/03
PB - Wiley
IS - 13
VL - 2022
SN - 1434-193X
SN - 1099-0690
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2022_Gribanov,
author = {Pavel S Gribanov and Daria V Vorobyeva and Sergey D Tokarev and Dmitry A Petropavlovskikh and Dmitry A Loginov and Sergey E. Nefedov and Fedor M. Dolgushin and Sergey N. Osipov},
title = {Rhodium‐Catalyzed C−H Activation/Annulation of Aryl Hydroxamates with Benzothiadiazol‐Containing Acetylenes: Access to Isoquinoline‐Bridged Donor‐Acceptor Luminophores},
journal = {European Journal of Organic Chemistry},
year = {2022},
volume = {2022},
publisher = {Wiley},
month = {apr},
url = {https://doi.org/10.1002/ejoc.202101572},
number = {13},
doi = {10.1002/ejoc.202101572}
}
Лаборатории