A New Convenient Synthesis of Alkoxyanthracenes from Alkoxy-9,10-anthraquinones
Publication type: Journal Article
Publication date: 2003-11-06
scimago Q2
wos Q2
SJR: 0.559
CiteScore: 4.6
Impact factor: 2.3
ISSN: 00397881, 1437210X
Catalysis
Organic Chemistry
Abstract
Methoxy-9,10-anthraquinones with mono-, di- and tetraether groups at different positions la-h can be directly reduced to the corresponding methoxyanthracenes 3a-h in moderate to good yields by zinc in refluxing acetic acid. Under similar conditions, ethyl I'-anthracenoxyacetate (3i) with the ester group unaffected and 1,8-oxybis(ethyleneoxyethyleneoxy)anthracene (5) were also conveniently synthesized in 65 and 70% yields, respectively.
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Chen C. et al. A New Convenient Synthesis of Alkoxyanthracenes from Alkoxy-9,10-anthraquinones // Synthesis. 2003. Vol. 16. pp. 2464-2466.
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Chen C., Chen Q., Zhu X., Chen C. A New Convenient Synthesis of Alkoxyanthracenes from Alkoxy-9,10-anthraquinones // Synthesis. 2003. Vol. 16. pp. 2464-2466.
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TY - JOUR
DO - 10.1055/s-2003-42408
UR - https://doi.org/10.1055/s-2003-42408
TI - A New Convenient Synthesis of Alkoxyanthracenes from Alkoxy-9,10-anthraquinones
T2 - Synthesis
AU - Chen, Chuanfeng
AU - Chen, Qiyin
AU - Zhu, Xiaozhang
AU - Chen, Chuanfeng
PY - 2003
DA - 2003/11/06
PB - Georg Thieme Verlag KG
SP - 2464-2466
IS - 16
SN - 0039-7881
SN - 1437-210X
ER -
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@article{2003_Chen,
author = {Chuanfeng Chen and Qiyin Chen and Xiaozhang Zhu and Chuanfeng Chen},
title = {A New Convenient Synthesis of Alkoxyanthracenes from Alkoxy-9,10-anthraquinones},
journal = {Synthesis},
year = {2003},
publisher = {Georg Thieme Verlag KG},
month = {nov},
url = {https://doi.org/10.1055/s-2003-42408},
number = {16},
pages = {2464--2466},
doi = {10.1055/s-2003-42408}
}