Chemical Communications, volume 48, issue 62, pages 7696
Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles
Publication type: Journal Article
Publication date: 2012-06-13
Journal:
Chemical Communications
Quartile SCImago
Q1
Quartile WOS
Q2
Impact factor: 4.9
ISSN: 13597345, 1364548X
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Abstract
A facile synthetic method of functionalized pyrrolo[1,2-a]indoles has been developed via a thermally-induced ring-opening and cyclization reaction from aniline-tethered alkylidenecyclopropanes with aldehydes.
Top-30
Citations by journals
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Angewandte Chemie - International Edition
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Angewandte Chemie
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2 publications, 4.26%
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1 publication, 2.13%
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Journal of Heterocyclic Chemistry
1 publication, 2.13%
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ChemInform
1 publication, 2.13%
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European Journal of Organic Chemistry
1 publication, 2.13%
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Chemical Reviews
1 publication, 2.13%
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Progress in Heterocyclic Chemistry
1 publication, 2.13%
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Organic Reaction Mechanisms
1 publication, 2.13%
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Russian Chemical Reviews
1 publication, 2.13%
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Citations by publishers
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Wiley
19 publications, 40.43%
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Royal Society of Chemistry (RSC)
15 publications, 31.91%
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American Chemical Society (ACS)
9 publications, 19.15%
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Elsevier
2 publications, 4.26%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.13%
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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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Chen K. et al. Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles // Chemical Communications. 2012. Vol. 48. No. 62. p. 7696.
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Chen K., Zhang Z., Wei Yin 尹., Shi M. Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles // Chemical Communications. 2012. Vol. 48. No. 62. p. 7696.
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TY - JOUR
DO - 10.1039/c2cc33269h
UR - https://doi.org/10.1039/c2cc33269h
TI - Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles
T2 - Chemical Communications
AU - Shi, Min
AU - Chen, Kai
AU - Zhang, Zhen
AU - Wei Yin, 尹维
PY - 2012
DA - 2012/06/13 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 7696
IS - 62
VL - 48
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex
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@article{2012_Chen,
author = {Min Shi and Kai Chen and Zhen Zhang and 尹维 Wei Yin},
title = {Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles},
journal = {Chemical Communications},
year = {2012},
volume = {48},
publisher = {Royal Society of Chemistry (RSC)},
month = {jun},
url = {https://doi.org/10.1039/c2cc33269h},
number = {62},
pages = {7696},
doi = {10.1039/c2cc33269h}
}
Cite this
MLA
Copy
Chen, Kai, et al. “Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles.” Chemical Communications, vol. 48, no. 62, Jun. 2012, p. 7696. https://doi.org/10.1039/c2cc33269h.