Chemical Communications, volume 58, issue 22, pages 3653-3656
Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes
Publication type: Journal Article
Publication date: 2022-02-19
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 ring-opening/cyclization cascade reaction of α-brominated amide-tethered alkylidenecyclopropanes in the presence of photocatalyst 4CzIPN under visible-light irradiation was developed to afford polycyclic benzazepine derivatives in good yields with broad substrate scope and good functional tolerance. A plausible mechanism involving a halogen atom transfer (XAT) process and a radical chain process is proposed for this reaction. This study provides a concise and practical strategy for the synthesis of benzazepine derivatives.
Top-30
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Chemical Communications
2 publications, 18.18%
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Tetrahedron Letters
1 publication, 9.09%
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Synfacts
1 publication, 9.09%
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European Journal of Organic Chemistry
1 publication, 9.09%
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Organic Chemistry Frontiers
1 publication, 9.09%
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ChemCatChem
1 publication, 9.09%
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Advanced Synthesis and Catalysis
1 publication, 9.09%
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Journal of Organic Chemistry
1 publication, 9.09%
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Russian Chemical Reviews
1 publication, 9.09%
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Chemical Science
1 publication, 9.09%
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2
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Citations by publishers
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1
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3
4
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Royal Society of Chemistry (RSC)
4 publications, 36.36%
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Wiley
3 publications, 27.27%
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Elsevier
1 publication, 9.09%
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Thieme
1 publication, 9.09%
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American Chemical Society (ACS)
1 publication, 9.09%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 9.09%
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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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Mao B. et al. Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes // Chemical Communications. 2022. Vol. 58. No. 22. pp. 3653-3656.
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Mao B., Zhang X., Wei Yin 尹., Shi M. Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes // Chemical Communications. 2022. Vol. 58. No. 22. pp. 3653-3656.
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TY - JOUR
DO - 10.1039/d1cc07136j
UR - https://doi.org/10.1039/d1cc07136j
TI - Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes
T2 - Chemical Communications
AU - Mao, Ben
AU - Zhang, Xiao-Yu
AU - Wei Yin, 尹维
AU - Shi, Min
PY - 2022
DA - 2022/02/19 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 3653-3656
IS - 22
VL - 58
SN - 1359-7345
SN - 1364-548X
ER -
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@article{2022_Mao,
author = {Ben Mao and Xiao-Yu Zhang and 尹维 Wei Yin and Min Shi},
title = {Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes},
journal = {Chemical Communications},
year = {2022},
volume = {58},
publisher = {Royal Society of Chemistry (RSC)},
month = {feb},
url = {https://doi.org/10.1039/d1cc07136j},
number = {22},
pages = {3653--3656},
doi = {10.1039/d1cc07136j}
}
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Mao, Ben, et al. “Visible-light-mediated intramolecular radical cyclization of α-brominated amide-tethered alkylidenecyclopropanes.” Chemical Communications, vol. 58, no. 22, Feb. 2022, pp. 3653-3656. https://doi.org/10.1039/d1cc07136j.