Journal of Organic Chemistry, volume 84, issue 14, pages 9282-9296
Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution
Publication type: Journal Article
Publication date: 2019-07-01
Journal:
Journal of Organic Chemistry
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
Abstract
A synthetic method for the construction of diiodinated all-carbon spirobiindene derivatives has been developed from the reaction of propargyl alcohol-tethered alkylidenecyclopropanes with iodine. The reaction proceeded through an iodination-initiated cascade intramolecular enyne cyclization and electrophilic aromatic substitution reaction process in 1,2-dichloroethane upon heating, giving desired spirocyclic products in moderate to excellent yields. Further transformation of the obtained products has also been presented.
Top-30
Citations by journals
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3 publications, 30%
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2 publications, 20%
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1 publication, 10%
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1 publication, 10%
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1 publication, 10%
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Chemical Communications
1 publication, 10%
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Russian Chemical Reviews
1 publication, 10%
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Citations by publishers
1
2
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4
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Royal Society of Chemistry (RSC)
4 publications, 40%
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American Chemical Society (ACS)
3 publications, 30%
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Wiley
2 publications, 20%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 10%
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2
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4
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- We do not take into account publications without a DOI.
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- Statistics recalculated weekly.
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Li Q. et al. Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution // Journal of Organic Chemistry. 2019. Vol. 84. No. 14. pp. 9282-9296.
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Li Q., Yu L., Wei Yin 尹., Shi M. Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution // Journal of Organic Chemistry. 2019. Vol. 84. No. 14. pp. 9282-9296.
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TY - JOUR
DO - 10.1021/acs.joc.9b01418
UR - https://doi.org/10.1021/acs.joc.9b01418
TI - Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution
T2 - Journal of Organic Chemistry
AU - Li, Quanzhe
AU - Yu, Liuzhu
AU - Wei Yin, 尹维
AU - Shi, Min
PY - 2019
DA - 2019/07/01 00:00:00
PB - American Chemical Society (ACS)
SP - 9282-9296
IS - 14
VL - 84
SN - 0022-3263
SN - 1520-6904
ER -
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@article{2019_Li,
author = {Quanzhe Li and Liuzhu Yu and 尹维 Wei Yin and Min Shi},
title = {Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution},
journal = {Journal of Organic Chemistry},
year = {2019},
volume = {84},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/acs.joc.9b01418},
number = {14},
pages = {9282--9296},
doi = {10.1021/acs.joc.9b01418}
}
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Li, Quanzhe, et al. “Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution.” Journal of Organic Chemistry, vol. 84, no. 14, Jul. 2019, pp. 9282-9296. https://doi.org/10.1021/acs.joc.9b01418.