| ID | 32963 |
| FullText URL | |
| Author |
Mamedov, Vakhid A.
Nurkhametova, Ilsiyar Z
Gubaidullin, Aidar T
Litvinov, Igor A
Tsuboi, Sadao
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| Abstract | Thiazolo[3,4-a]quinoxalin-4-ones were prepared in two steps starting from methyl phenylchloropyruvate using a new strategy for the construction of the ring system. A key step in this new method involves the reaction of 4-hydroxytetrahydrothiazoles with 1,2-phenylendiamines.
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| Keywords | chlorophenylpyruvate
thiazoline
thiazole
alpha-halo ketone
1
2-phenylenediamine
NITROGEN
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| Note | Published with permission from the copyright holder.
This is the institute's copy, as published in
the Journal of Heterocycles, August 2004, Volume 63, Issue 8, Pages 1783-1792.
Direct access to Thomson Web of Science record Copyright © 2004 The Japan Institute of Heterocyclic Chemistry. All rights reserved. |
| Published Date | 2004-08-01
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| Publication Title |
Heterocycles
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| Volume | volume63
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| Issue | issue8
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| Start Page | 1783
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| End Page | 1792
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| Content Type |
Journal Article
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| language |
English
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| OAI-PMH Set |
岡山大学
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| DOI | |
| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.3987/com-04-10084
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