Open Access
Open access
том 1 издание 9 страницы 1745

Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids

Тип публикацииJournal Article
Дата публикации2011-10-25
scimago Q1
wos Q2
БС1
SJR0.777
CiteScore7.6
Impact factor4.6
ISSN20462069
General Chemistry
General Chemical Engineering
Краткое описание
Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10-anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones – substituted analogues of Aporphinoid alkaloids.
Найдено 
Для доступа к списку цитирований публикации необходимо авторизоваться.
Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.

Топ-30

Журналы

1
2
3
4
Journal of Organic Chemistry
4 публикации, 17.39%
Molecules
2 публикации, 8.7%
Chemistry of Heterocyclic Compounds
2 публикации, 8.7%
Mendeleev Communications
2 публикации, 8.7%
Chemistry - A European Journal
2 публикации, 8.7%
Australian Journal of Chemistry
1 публикация, 4.35%
Russian Chemical Reviews
1 публикация, 4.35%
International Turfgrass Society Research Journal
1 публикация, 4.35%
European Journal of Organic Chemistry
1 публикация, 4.35%
Organic Process Research and Development
1 публикация, 4.35%
Organic Letters
1 публикация, 4.35%
Chemical Reviews
1 публикация, 4.35%
Chemical Society Reviews
1 публикация, 4.35%
Russian Journal of General Chemistry
1 публикация, 4.35%
Журнал Общей Химии
1 публикация, 4.35%
International Journal of Molecular Sciences
1 публикация, 4.35%
1
2
3
4

Издатели

1
2
3
4
5
6
7
American Chemical Society (ACS)
7 публикаций, 30.43%
Wiley
4 публикации, 17.39%
MDPI
3 публикации, 13.04%
Springer Nature
2 публикации, 8.7%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
2 публикации, 8.7%
Pleiades Publishing
2 публикации, 8.7%
CSIRO Publishing
1 публикация, 4.35%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 4.35%
Royal Society of Chemistry (RSC)
1 публикация, 4.35%
1
2
3
4
5
6
7
  • 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
23
Поделиться
Цитировать
ГОСТ |
Цитировать
Krasnok A. E. et al. Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids // RSC Advances. 2011. Vol. 1. No. 9. p. 1745.
ГОСТ со всеми авторами (до 50) Скопировать
Krasnok A. E., Vasilevsky S. F., Gold B., Alabugin I. V. Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids // RSC Advances. 2011. Vol. 1. No. 9. p. 1745.
RIS |
Цитировать
TY - JOUR
DO - 10.1039/c1ra00622c
UR - https://doi.org/10.1039/c1ra00622c
TI - Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids
T2 - RSC Advances
AU - Krasnok, A E
AU - Vasilevsky, Sergei F.
AU - Gold, Brian
AU - Alabugin, Igor V.
PY - 2011
DA - 2011/10/25
PB - Royal Society of Chemistry (RSC)
SP - 1745
IS - 9
VL - 1
SN - 2046-2069
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2011_Krasnok,
author = {A E Krasnok and Sergei F. Vasilevsky and Brian Gold and Igor V. Alabugin},
title = {Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids},
journal = {RSC Advances},
year = {2011},
volume = {1},
publisher = {Royal Society of Chemistry (RSC)},
month = {oct},
url = {https://doi.org/10.1039/c1ra00622c},
number = {9},
pages = {1745},
doi = {10.1039/c1ra00622c}
}
MLA
Цитировать
Krasnok, A. E., et al. “Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids.” RSC Advances, vol. 1, no. 9, Oct. 2011, p. 1745. https://doi.org/10.1039/c1ra00622c.