One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination
Publication type: Journal Article
Publication date: 2016-01-01
scimago Q2
wos Q2
SJR: 0.600
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
26542026
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
We have developed a highly efficient synthetic route to carbazoles that employs sequential C–C/C–N bond formation
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Metrics
36
Total citations:
36
Citations from 2024:
10
(27.77%)
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MLA
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GOST
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Goo D. Y., Goo D., Woo S. K. One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination // Organic and Biomolecular Chemistry. 2016. Vol. 14. No. 1. pp. 122-130.
GOST all authors (up to 50)
Copy
Goo D. Y., Goo D., Woo S. K. One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination // Organic and Biomolecular Chemistry. 2016. Vol. 14. No. 1. pp. 122-130.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c5ob01952d
UR - https://doi.org/10.1039/c5ob01952d
TI - One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination
T2 - Organic and Biomolecular Chemistry
AU - Goo, Deuk Young
AU - Goo, Deuk-Young
AU - Woo, Sang Kook
PY - 2016
DA - 2016/01/01
PB - Royal Society of Chemistry (RSC)
SP - 122-130
IS - 1
VL - 14
PMID - 26542026
SN - 1477-0520
SN - 1477-0539
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2016_Goo,
author = {Deuk Young Goo and Deuk-Young Goo and Sang Kook Woo},
title = {One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination},
journal = {Organic and Biomolecular Chemistry},
year = {2016},
volume = {14},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c5ob01952d},
number = {1},
pages = {122--130},
doi = {10.1039/c5ob01952d}
}
Cite this
MLA
Copy
Goo, Deuk Young, et al. “One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination.” Organic and Biomolecular Chemistry, vol. 14, no. 1, Jan. 2016, pp. 122-130. https://doi.org/10.1039/c5ob01952d.