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HERO ID
5177558
Reference Type
Journal Article
Title
Short-step synthesis of 1,3-disubstituted naphtho 2,3-c furan-4,9-dione and naphtho 2,3-b furan-4,9-dione by the Friedel-Crafts reaction
Author(s)
Koyama, J; Toyokuni, I; Kino, A; Tagahara, K
Year
1998
Is Peer Reviewed?
Yes
Journal
Heterocycles
ISSN:
0385-5414
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Location
OXFORD
Volume
48
Issue
8
Page Numbers
1631-1638
Language
English
DOI
10.3987/com-98-8172
Web of Science Id
WOS:000075542500014
URL
http://
://CCC:000075542500014http://www.elsevier.com
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Abstract
1,3-Dialkylnaphtho[2,3-c] furan-4,9-diones were obtained by the Friedel-Crafts reaction of phthalic anhydride with 2,5-dialkylfurans. The reaction of phthalic anhydride with 2-acetyl-5-methylfuran, instead of 2,5-dialkylfurans, produced 2-methylnaphtho[2,3-b] furan-4,9-dione. The application of this method to the synthesis of 8-hydroxynaphtho [2, 3-b] furan-4, 9-dione [isodiodantunezone] is also described.
Keywords
Polymer Science; barr-virus-activation, cyto-toxic quinones, agents
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