том 19 издание 19 страницы 5284-5287

Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction

Тип публикацииJournal Article
Дата публикации2017-09-14
scimago Q1
wos Q1
БС1
SJR1.235
CiteScore8.7
Impact factor5.0
ISSN15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
A tandem [3 + 2] cycloaddition/reductive cyclization of nitrochalcones with activated methylene isocyanides for the efficient synthesis of pyrrolo[2,3-b]quinolones is reported. In this reaction, the in situ generated dihydropyrroline acts as the internal reductant to convert the nitro into an electrophilic nitroso group, which undergoes subsequent C-N bond formation. Transition-metal-free, simple experimental procedure and ready accessibility of starting materials characterize the present transformation.
Найдено 
Найдено 

Топ-30

Журналы

2
4
6
8
10
12
Organic Letters
11 публикаций, 25.58%
Journal of Organic Chemistry
5 публикаций, 11.63%
Organic and Biomolecular Chemistry
3 публикации, 6.98%
Organic Chemistry Frontiers
3 публикации, 6.98%
ChemistrySelect
2 публикации, 4.65%
Asian Journal of Organic Chemistry
2 публикации, 4.65%
Advanced Synthesis and Catalysis
2 публикации, 4.65%
Crystals
1 публикация, 2.33%
Molecules
1 публикация, 2.33%
Chinese Journal of Catalysis
1 публикация, 2.33%
Tetrahedron
1 публикация, 2.33%
Applied Organometallic Chemistry
1 публикация, 2.33%
Chemistry - A European Journal
1 публикация, 2.33%
Chemistry - An Asian Journal
1 публикация, 2.33%
European Journal of Organic Chemistry
1 публикация, 2.33%
RSC Advances
1 публикация, 2.33%
Chemical Communications
1 публикация, 2.33%
Synthesis
1 публикация, 2.33%
Journal of Agricultural and Food Chemistry
1 публикация, 2.33%
Russian Chemical Reviews
1 публикация, 2.33%
MolBank
1 публикация, 2.33%
Green Chemistry
1 публикация, 2.33%
2
4
6
8
10
12

Издатели

2
4
6
8
10
12
14
16
18
American Chemical Society (ACS)
17 публикаций, 39.53%
Wiley
10 публикаций, 23.26%
Royal Society of Chemistry (RSC)
9 публикаций, 20.93%
MDPI
3 публикации, 6.98%
Elsevier
2 публикации, 4.65%
Georg Thieme Verlag KG
1 публикация, 2.33%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 2.33%
2
4
6
8
10
12
14
16
18
  • 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
43
Поделиться
Цитировать
ГОСТ |
Цитировать
Lin Z. et al. Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction // Organic Letters. 2017. Vol. 19. No. 19. pp. 5284-5287.
ГОСТ со всеми авторами (до 50) Скопировать
Lin Z., Hu Z., Zhang X., Dong J., Liu J., Chen D., Xu X. Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction // Organic Letters. 2017. Vol. 19. No. 19. pp. 5284-5287.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/acs.orglett.7b02558
UR - https://doi.org/10.1021/acs.orglett.7b02558
TI - Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction
T2 - Organic Letters
AU - Lin, Zhichen
AU - Hu, Zhongyan
AU - Zhang, Xin
AU - Dong, Jinhuan
AU - Liu, Jian-Biao
AU - Chen, De-Zhan
AU - Xu, Xianxiu
PY - 2017
DA - 2017/09/14
PB - American Chemical Society (ACS)
SP - 5284-5287
IS - 19
VL - 19
PMID - 28910113
SN - 1523-7060
SN - 1523-7052
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2017_Lin,
author = {Zhichen Lin and Zhongyan Hu and Xin Zhang and Jinhuan Dong and Jian-Biao Liu and De-Zhan Chen and Xianxiu Xu},
title = {Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction},
journal = {Organic Letters},
year = {2017},
volume = {19},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/acs.orglett.7b02558},
number = {19},
pages = {5284--5287},
doi = {10.1021/acs.orglett.7b02558}
}
MLA
Цитировать
Lin, Zhichen, et al. “Tandem Synthesis of Pyrrolo[2,3-b]quinolones via Cadogen-Type Reaction.” Organic Letters, vol. 19, no. 19, Sep. 2017, pp. 5284-5287. https://doi.org/10.1021/acs.orglett.7b02558.