Organic Letters, volume 10, issue 23, pages 5481-5484
Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters
Publication type: Journal Article
Publication date: 2008-11-08
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
The first Friedel-Crafts reaction initiated by the direct generation of a carbocation at the C3 position of MCP 1,1-diesters through distal-bond cleavage was presented. The described method supplied a new synthetic strategy to prepare indene and hydronaphthalene derivatives in moderate to excellent yields under mild conditions.
Top-30
Citations by journals
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Organic Letters
9 publications, 16.67%
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European Journal of Organic Chemistry
7 publications, 12.96%
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Tetrahedron
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Journal of Organic Chemistry
5 publications, 9.26%
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Chemical Communications
4 publications, 7.41%
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Advanced Synthesis and Catalysis
3 publications, 5.56%
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Tetrahedron Letters
2 publications, 3.7%
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Journal of the American Chemical Society
2 publications, 3.7%
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Chemical Reviews
2 publications, 3.7%
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Synlett
2 publications, 3.7%
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Asian Journal of Organic Chemistry
1 publication, 1.85%
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Chemistry - A European Journal
1 publication, 1.85%
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ChemInform
1 publication, 1.85%
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RSC Advances
1 publication, 1.85%
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Organic Chemistry Frontiers
1 publication, 1.85%
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Organic and Biomolecular Chemistry
1 publication, 1.85%
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Organic Preparations and Procedures International
1 publication, 1.85%
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Catalysts
1 publication, 1.85%
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Synthesis
1 publication, 1.85%
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Russian Chemical Reviews
1 publication, 1.85%
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Citations by publishers
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2
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18
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American Chemical Society (ACS)
18 publications, 33.33%
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Wiley
16 publications, 29.63%
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Elsevier
7 publications, 12.96%
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Royal Society of Chemistry (RSC)
7 publications, 12.96%
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Thieme
3 publications, 5.56%
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Taylor & Francis
1 publication, 1.85%
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Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 1.85%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.85%
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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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Hu B., Xing S., Wang Z. Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters // Organic Letters. 2008. Vol. 10. No. 23. pp. 5481-5484.
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Hu B., Xing S., Wang Z. Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters // Organic Letters. 2008. Vol. 10. No. 23. pp. 5481-5484.
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TY - JOUR
DO - 10.1021/ol802301e
UR - https://doi.org/10.1021/ol802301e
TI - Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters
T2 - Organic Letters
AU - Hu, Bao
AU - Xing, Siyang
AU - Wang, Zhong-Wen
PY - 2008
DA - 2008/11/08 00:00:00
PB - American Chemical Society (ACS)
SP - 5481-5484
IS - 23
VL - 10
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
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@article{2008_Hu,
author = {Bao Hu and Siyang Xing and Zhong-Wen Wang},
title = {Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters},
journal = {Organic Letters},
year = {2008},
volume = {10},
publisher = {American Chemical Society (ACS)},
month = {nov},
url = {https://doi.org/10.1021/ol802301e},
number = {23},
pages = {5481--5484},
doi = {10.1021/ol802301e}
}
Cite this
MLA
Copy
Hu, Bao, et al. “Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters.” Organic Letters, vol. 10, no. 23, Nov. 2008, pp. 5481-5484. https://doi.org/10.1021/ol802301e.