Journal of Organic Chemistry, volume 69, issue 16, pages 5471-5472
First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters
Publication type: Journal Article
Publication date: 2004-07-03
Journal:
Journal of Organic Chemistry
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
Abstract
Alkylidenecyclopropanes undergo Mn(OAc)3-mediated addition with malonate, leading to dihydronaphthalene derivatives in moderate yields.
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1 publication, 1.92%
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1
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5
6
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Citations by publishers
2
4
6
8
10
12
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Wiley
12 publications, 23.08%
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American Chemical Society (ACS)
10 publications, 19.23%
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Elsevier
9 publications, 17.31%
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Royal Society of Chemistry (RSC)
9 publications, 17.31%
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Thieme
5 publications, 9.62%
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Springer Nature
2 publications, 3.85%
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Beilstein-Institut
1 publication, 1.92%
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Taylor & Francis
1 publication, 1.92%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.92%
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2
4
6
8
10
12
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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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Zhou H., Huang X., Chen W. First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters // Journal of Organic Chemistry. 2004. Vol. 69. No. 16. pp. 5471-5472.
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Zhou H., Huang X., Chen W. First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters // Journal of Organic Chemistry. 2004. Vol. 69. No. 16. pp. 5471-5472.
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TY - JOUR
DO - 10.1021/jo0496289
UR - https://doi.org/10.1021/jo0496289
TI - First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters
T2 - Journal of Organic Chemistry
AU - Huang, Xian
AU - Chen, Wanli
AU - Zhou, Hongwei
PY - 2004
DA - 2004/07/03 00:00:00
PB - American Chemical Society (ACS)
SP - 5471-5472
IS - 16
VL - 69
SN - 0022-3263
SN - 1520-6904
ER -
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@article{2004_Zhou,
author = {Xian Huang and Wanli Chen and Hongwei Zhou},
title = {First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters},
journal = {Journal of Organic Chemistry},
year = {2004},
volume = {69},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/jo0496289},
number = {16},
pages = {5471--5472},
doi = {10.1021/jo0496289}
}
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Zhou, Hongwei, et al. “First Tandem Free-Radical Cyclization Reaction of Alkylenecyclopropanes: A Novel and Efficient Method for the Preparation of 2-(3,4-Dihydronaphthalen-2-yl)malonic Acid Diethyl Esters.” Journal of Organic Chemistry, vol. 69, no. 16, Jul. 2004, pp. 5471-5472. https://doi.org/10.1021/jo0496289.