Open Access
Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group
1
School of Chemical Engineering
2
YeungNam University
3
Gyeongsan 712-749
|
4
Republic of Korea
|
Publication type: Journal Article
Publication date: 2015-09-16
scimago Q1
wos Q1
SJR: 2.138
CiteScore: 12.6
Impact factor: 7.4
ISSN: 20416520, 20416539
PubMed ID:
29861941
General Chemistry
Abstract
A transition-metal-free unique tandem annulation reaction has been developed for the synthesis of various functionalized 3-hydroxycarbazoles.
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Metrics
80
Total citations:
80
Citations from 2024:
12
(15%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Poudel T. N. et al. Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group // Chemical Science. 2015. Vol. 6. No. 12. pp. 7028-7033.
GOST all authors (up to 50)
Copy
Poudel T. N., Lee Y. B. Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group // Chemical Science. 2015. Vol. 6. No. 12. pp. 7028-7033.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c5sc02407b
UR - https://doi.org/10.1039/c5sc02407b
TI - Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group
T2 - Chemical Science
AU - Poudel, Tej Narayan
AU - Lee, Yong Beom
PY - 2015
DA - 2015/09/16
PB - Royal Society of Chemistry (RSC)
SP - 7028-7033
IS - 12
VL - 6
PMID - 29861941
SN - 2041-6520
SN - 2041-6539
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2015_Poudel,
author = {Tej Narayan Poudel and Yong Beom Lee},
title = {Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group},
journal = {Chemical Science},
year = {2015},
volume = {6},
publisher = {Royal Society of Chemistry (RSC)},
month = {sep},
url = {https://doi.org/10.1039/c5sc02407b},
number = {12},
pages = {7028--7033},
doi = {10.1039/c5sc02407b}
}
Cite this
MLA
Copy
Poudel, Tej Narayan, et al. “Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group.” Chemical Science, vol. 6, no. 12, Sep. 2015, pp. 7028-7033. https://doi.org/10.1039/c5sc02407b.