Studies on heterocyclic analogs of azulenes. IV. Behavior of 2-chlorocyclohepta[b]pyrrole derivatives toward phosphorus ylide.
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概要
- 論文の詳細を見る
The transylidation reaction of methyl(triphenylphosphoranylidene)acetate with 2-chlorocyclohepta[<I>b</I>]pyrrole derivatives has been studied. 3,8-Disubstituted derivatives gave a transylidation product only, whereas 3-substituted derivatives afforded not only a transylidation products but also the compounds formed by the addition of ylide at C-8. <SUP>13</SUP>C NMR spectra of the transylidation products are recorded in part.
- 公益社団法人 日本化学会の論文
著者
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Abe Noritaka
Department Of Pure And Applied Chemistry Faculty Of Science And Technology Tokyo University Of Scien
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Nishiwaki Tarozaemon
Department of Chemistry, Yamaguchi University
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Nishiwaki Tarozaemon
Department of Chemistry, Faculty of Science, Yamaguchi University
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Miura Kaoru
Department of Chemistry, Yamaguchi University
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Ishida Kozue
Department of Chemistry, Yamaguchi University
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