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Diels—Alder Reaction of 1-Methyl-3,6,8-trinitro-2-quinolone.

✍ Scribed by Motoki Asahara; Moriaki Nagamatsu; Yasuo Tohda; Nagatoshi Nishiwaki; Masahiro Ariga

Publisher
John Wiley and Sons
Year
2005
Weight
18 KB
Volume
36
Category
Article
ISSN
0931-7597

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Diels-alder reaction of 1-methyl-3,6,8-t
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✍ Motoki Asahara; Moriaki Nagamatsu; Yasuo Tohda; Nagatoshi Nishiwaki; Masahiro Ar 📂 Article 📅 2004 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 111 KB

## Abstract 1‐Methyl‐3,6,8‐trinitro‐2‐quinolone **(1)** behaved as the dienophile in Diels‐Alder reactions with dienes. When cyclopentadiene was used, cycloadduct **4** was obtained, which was then aromatized on treatment with triethylamine. In the reaction of **1** with hydrazone of 2‐butenal, phe

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ChemInform Abstract: Diels—Alder Reaction of 1,3-Butadiene Derivatives with 1-Methyl-2(1H)-quinolones Having an Electron-Withdrawing Group at the 4-Position.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v