Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes
Тип публикации: Journal Article
Дата публикации: 2017-09-01
scimago Q3
wos Q3
БС2
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
A series of polysubstituted furans and dihydrofurans have been prepared from readily available oxodienes and bromonitromethane in modest to excellent yields. This facile synthetic method is developed on the basis of proprietary properties of nitro group such as strong electron-withdrawing ability and cleavability. The conversion of nitro-substituted dihydrofurans to furans is presumably realized by elimination of HNO 2 under the aid of DABCO.
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Для доступа к списку цитирований публикации необходимо авторизоваться.
Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.
Топ-30
Журналы
|
1
2
3
|
|
|
European Journal of Organic Chemistry
3 публикации, 17.65%
|
|
|
Chemistry of Heterocyclic Compounds
2 публикации, 11.76%
|
|
|
ChemistrySelect
2 публикации, 11.76%
|
|
|
Organic and Biomolecular Chemistry
2 публикации, 11.76%
|
|
|
Beilstein Journal of Organic Chemistry
1 публикация, 5.88%
|
|
|
Mini-Reviews in Organic Chemistry
1 публикация, 5.88%
|
|
|
Reactions
1 публикация, 5.88%
|
|
|
Tetrahedron Letters
1 публикация, 5.88%
|
|
|
ACS Omega
1 публикация, 5.88%
|
|
|
Journal of Organic Chemistry
1 публикация, 5.88%
|
|
|
Organic Preparations and Procedures International
1 публикация, 5.88%
|
|
|
Progress in Heterocyclic Chemistry
1 публикация, 5.88%
|
|
|
1
2
3
|
Издатели
|
1
2
3
4
5
|
|
|
Wiley
5 публикаций, 29.41%
|
|
|
Springer Nature
2 публикации, 11.76%
|
|
|
Elsevier
2 публикации, 11.76%
|
|
|
American Chemical Society (ACS)
2 публикации, 11.76%
|
|
|
Royal Society of Chemistry (RSC)
2 публикации, 11.76%
|
|
|
Beilstein-Institut
1 публикация, 5.88%
|
|
|
Bentham Science Publishers Ltd.
1 публикация, 5.88%
|
|
|
MDPI
1 публикация, 5.88%
|
|
|
Taylor & Francis
1 публикация, 5.88%
|
|
|
1
2
3
4
5
|
- 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
17
Всего цитирований:
17
Цитирований c 2025:
1
(5.88%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Chen R. et al. Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes // Tetrahedron Letters. 2017. Vol. 58. No. 38. pp. 3722-3726.
ГОСТ со всеми авторами (до 50)
Скопировать
Chen R., Xia F., Xu Z., He Z. Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes // Tetrahedron Letters. 2017. Vol. 58. No. 38. pp. 3722-3726.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1016/j.tetlet.2017.08.027
UR - https://doi.org/10.1016/j.tetlet.2017.08.027
TI - Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes
T2 - Tetrahedron Letters
AU - Chen, Rongshun
AU - Xia, Fan
AU - Xu, Zhaozhong
AU - He, Zhengjie
PY - 2017
DA - 2017/09/01
PB - Elsevier
SP - 3722-3726
IS - 38
VL - 58
SN - 0040-4039
SN - 1873-3581
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2017_Chen,
author = {Rongshun Chen and Fan Xia and Zhaozhong Xu and Zhengjie He},
title = {Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes},
journal = {Tetrahedron Letters},
year = {2017},
volume = {58},
publisher = {Elsevier},
month = {sep},
url = {https://doi.org/10.1016/j.tetlet.2017.08.027},
number = {38},
pages = {3722--3726},
doi = {10.1016/j.tetlet.2017.08.027}
}
Цитировать
MLA
Скопировать
Chen, Rongshun, et al. “Facile synthesis of polysubstituted furans and dihydrofurans via cyclization of bromonitromethane with oxodienes.” Tetrahedron Letters, vol. 58, no. 38, Sep. 2017, pp. 3722-3726. https://doi.org/10.1016/j.tetlet.2017.08.027.