Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles
Publication type: Journal Article
Publication date: 2016-11-18
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
27934374
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
A simple Brønsted acid catalyzed tandem reaction, including intermolecular nucleophilic addition, substitution and intramolecular cyclization, in a one-pot manner is described. Thirty two 2-indolyl substituted carbazoles are generated in good to excellent yields. Based on this tandem reaction strategy, the poly(1,4-carbazole) is prepared for the first time. Preliminary studies indicate that the poly(1,4-carbazole) has good thermostability and optical properties.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
3
4
5
6
|
|
|
Journal of Organic Chemistry
6 publications, 20%
|
|
|
Organic Letters
5 publications, 16.67%
|
|
|
Advanced Synthesis and Catalysis
2 publications, 6.67%
|
|
|
Organic Chemistry Frontiers
2 publications, 6.67%
|
|
|
Monatshefte fur Chemie
1 publication, 3.33%
|
|
|
Chinese Chemical Letters
1 publication, 3.33%
|
|
|
Journal of Organometallic Chemistry
1 publication, 3.33%
|
|
|
ChemCatChem
1 publication, 3.33%
|
|
|
Chemical Communications
1 publication, 3.33%
|
|
|
Organic and Biomolecular Chemistry
1 publication, 3.33%
|
|
|
Green Chemistry
1 publication, 3.33%
|
|
|
Progress in Heterocyclic Chemistry
1 publication, 3.33%
|
|
|
Advances in Heterocyclic Chemistry
1 publication, 3.33%
|
|
|
Materials Today Chemistry
1 publication, 3.33%
|
|
|
Current Organic Chemistry
1 publication, 3.33%
|
|
|
Russian Chemical Reviews
1 publication, 3.33%
|
|
|
Archiv der Pharmazie
1 publication, 3.33%
|
|
|
1
2
3
4
5
6
|
Publishers
|
2
4
6
8
10
12
|
|
|
American Chemical Society (ACS)
11 publications, 36.67%
|
|
|
Elsevier
7 publications, 23.33%
|
|
|
Royal Society of Chemistry (RSC)
5 publications, 16.67%
|
|
|
Wiley
4 publications, 13.33%
|
|
|
Springer Nature
1 publication, 3.33%
|
|
|
Bentham Science Publishers Ltd.
1 publication, 3.33%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 3.33%
|
|
|
2
4
6
8
10
12
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
30
Total citations:
30
Citations from 2024:
4
(13.33%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Huang Y. et al. Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles // Organic Letters. 2016. Vol. 18. No. 23. pp. 6200-6203.
GOST all authors (up to 50)
Copy
Huang Y., LI Xiao-yun X., Fu L., Guo Q. X. Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles // Organic Letters. 2016. Vol. 18. No. 23. pp. 6200-6203.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/acs.orglett.6b03257
UR - https://doi.org/10.1021/acs.orglett.6b03257
TI - Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles
T2 - Organic Letters
AU - Huang, Yi-Wei
AU - LI Xiao-yun, Xiao-Yun
AU - Fu, Li-Na
AU - Guo, Qi Xiang
PY - 2016
DA - 2016/11/18
PB - American Chemical Society (ACS)
SP - 6200-6203
IS - 23
VL - 18
PMID - 27934374
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2016_Huang,
author = {Yi-Wei Huang and Xiao-Yun LI Xiao-yun and Li-Na Fu and Qi Xiang Guo},
title = {Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles},
journal = {Organic Letters},
year = {2016},
volume = {18},
publisher = {American Chemical Society (ACS)},
month = {nov},
url = {https://doi.org/10.1021/acs.orglett.6b03257},
number = {23},
pages = {6200--6203},
doi = {10.1021/acs.orglett.6b03257}
}
Cite this
MLA
Copy
Huang, Yi-Wei, et al. “Procedure for the Synthesis of Polysubstituted Carbazoles from 3-Vinyl Indoles.” Organic Letters, vol. 18, no. 23, Nov. 2016, pp. 6200-6203. https://doi.org/10.1021/acs.orglett.6b03257.