Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols.
Publication type: Journal Article
Publication date: 2012-12-10
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
23228044
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
AuCl(3)-catalyzed reaction of 1-(indol-2-yl)-3-alkyn-1-ols occurred smoothly in toluene at room temperature to form a benzene ring leading to a series of carbazole derivatives efficiently. A possible mechanism has been proposed for the formation of carbazoles.
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116
Total citations:
116
Citations from 2024:
8
(6.9%)
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GOST
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Qiu Y. et al. Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols. // Organic Letters. 2012. Vol. 14. No. 24. pp. 6198-6201.
GOST all authors (up to 50)
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Qiu Y., Kong W., FU C., Ma S. Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols. // Organic Letters. 2012. Vol. 14. No. 24. pp. 6198-6201.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol3029498
UR - https://doi.org/10.1021/ol3029498
TI - Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols.
T2 - Organic Letters
AU - Qiu, Youai
AU - Kong, Wangqing
AU - FU, CHUNLING
AU - Ma, Sheng-Ming
PY - 2012
DA - 2012/12/10
PB - American Chemical Society (ACS)
SP - 6198-6201
IS - 24
VL - 14
PMID - 23228044
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2012_Qiu,
author = {Youai Qiu and Wangqing Kong and CHUNLING FU and Sheng-Ming Ma},
title = {Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols.},
journal = {Organic Letters},
year = {2012},
volume = {14},
publisher = {American Chemical Society (ACS)},
month = {dec},
url = {https://doi.org/10.1021/ol3029498},
number = {24},
pages = {6198--6201},
doi = {10.1021/ol3029498}
}
Cite this
MLA
Copy
Qiu, Youai, et al. “Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols..” Organic Letters, vol. 14, no. 24, Dec. 2012, pp. 6198-6201. https://doi.org/10.1021/ol3029498.