Organic Chemistry Frontiers, volume 3, issue 10, pages 1299-1303
An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions
Cheng Guo Liu
1
,
Cheng-guo Liu
1
,
Zheng Yang Gu
1
,
Zheng-Yang Gu
1
,
Hui Wen Bai
1
,
Hui-Wen Bai
1
,
Shun-Yi Wang
1
,
Shunjun Ji
1
Publication type: Journal Article
Publication date: 2016-08-08
Journal:
Organic Chemistry Frontiers
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.4
ISSN: 20524110, 20524129
Organic Chemistry
Abstract
An isocyanide insertion approach to construct the pyrrolo[2,3-
Top-30
Citations by journals
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Journal of Organic Chemistry
2 publications, 10.53%
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New Journal of Chemistry
2 publications, 10.53%
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European Journal of Organic Chemistry
1 publication, 5.26%
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Chemistry - A European Journal
1 publication, 5.26%
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Organic Chemistry Frontiers
1 publication, 5.26%
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Organic and Biomolecular Chemistry
1 publication, 5.26%
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Chemical Society Reviews
1 publication, 5.26%
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Synthetic Communications
1 publication, 5.26%
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Asian Journal of Organic Chemistry
1 publication, 5.26%
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Russian Chemical Reviews
1 publication, 5.26%
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Citations by publishers
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1
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3
4
5
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7
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Wiley
7 publications, 36.84%
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American Chemical Society (ACS)
5 publications, 26.32%
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Royal Society of Chemistry (RSC)
5 publications, 26.32%
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Taylor & Francis
1 publication, 5.26%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 5.26%
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- We do not take into account publications without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Liu C. G. et al. An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions // Organic Chemistry Frontiers. 2016. Vol. 3. No. 10. pp. 1299-1303.
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Liu C. G., Liu C., Gu Z. Y., Gu Z., Bai H. W., Bai H., Wang S., Ji S. An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions // Organic Chemistry Frontiers. 2016. Vol. 3. No. 10. pp. 1299-1303.
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TY - JOUR
DO - 10.1039/c6qo00373g
UR - https://doi.org/10.1039/c6qo00373g
TI - An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions
T2 - Organic Chemistry Frontiers
AU - Liu, Cheng Guo
AU - Gu, Zheng Yang
AU - Bai, Hui Wen
AU - Wang, Shun-Yi
AU - Ji, Shunjun
AU - Liu, Cheng-guo
AU - Gu, Zheng-Yang
AU - Bai, Hui-Wen
PY - 2016
DA - 2016/08/08 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 1299-1303
IS - 10
VL - 3
SN - 2052-4110
SN - 2052-4129
ER -
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@article{2016_Liu,
author = {Cheng Guo Liu and Zheng Yang Gu and Hui Wen Bai and Shun-Yi Wang and Shunjun Ji and Cheng-guo Liu and Zheng-Yang Gu and Hui-Wen Bai},
title = {An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions},
journal = {Organic Chemistry Frontiers},
year = {2016},
volume = {3},
publisher = {Royal Society of Chemistry (RSC)},
month = {aug},
url = {https://doi.org/10.1039/c6qo00373g},
number = {10},
pages = {1299--1303},
doi = {10.1039/c6qo00373g}
}
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Liu, Cheng Guo, et al. “An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions.” Organic Chemistry Frontiers, vol. 3, no. 10, Aug. 2016, pp. 1299-1303. https://doi.org/10.1039/c6qo00373g.
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