Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines
Publication type: Journal Article
Publication date: 2011-08-22
scimago Q2
wos Q1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
PubMed ID:
21819061
Organic Chemistry
Abstract
Selective synthesis of quinolines has been achieved via oxidative annulation of functionalized pyridines with two alkyne molecules under Rh(III)-catalyzed cascade C-H activation of pyridines using Cu(OAc)(2) as an oxidant. The selectivity of this reaction is oxidant-dependent, particularly on the anion of the oxidant.
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Metrics
164
Total citations:
164
Citations from 2024:
7
(4.27%)
Cite this
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MLA
Cite this
GOST
Copy
Song G., Gong X., Li X. Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines // Journal of Organic Chemistry. 2011. Vol. 76. No. 18. pp. 7583-7589.
GOST all authors (up to 50)
Copy
Song G., Gong X., Li X. Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines // Journal of Organic Chemistry. 2011. Vol. 76. No. 18. pp. 7583-7589.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/jo201266u
UR - https://doi.org/10.1021/jo201266u
TI - Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines
T2 - Journal of Organic Chemistry
AU - Song, Guoyong
AU - Gong, Xue
AU - Li, Xingwei
PY - 2011
DA - 2011/08/22
PB - American Chemical Society (ACS)
SP - 7583-7589
IS - 18
VL - 76
PMID - 21819061
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2011_Song,
author = {Guoyong Song and Xue Gong and Xingwei Li},
title = {Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines},
journal = {Journal of Organic Chemistry},
year = {2011},
volume = {76},
publisher = {American Chemical Society (ACS)},
month = {aug},
url = {https://doi.org/10.1021/jo201266u},
number = {18},
pages = {7583--7589},
doi = {10.1021/jo201266u}
}
Cite this
MLA
Copy
Song, Guoyong, et al. “Synthesis of Quinolines via Rh(III)-Catalyzed Oxidative Annulation of Pyridines.” Journal of Organic Chemistry, vol. 76, no. 18, Aug. 2011, pp. 7583-7589. https://doi.org/10.1021/jo201266u.