Nonacarbonyldiiron-induced reaction of 3-azido-1,2,3-triphenyl-cyclopropene and 4,5,6-triphenyl-1,2,3-triazine.
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概要
- 論文の詳細を見る
The [Fe<SUB>2</SUB>(CO)<SUB>9</SUB>]-induced reaction of 3-azido-1,2,3-triphenylcyclopropene (<B>1</B>) undergoes elimination of a nitrogen molecule and C–C bond cleavage to result in the formation of benzonitrile, diphenylacetylene, 2,3-diphenylinden-1-one, and 1,2,3-triphenylpropen-1-one. The similar reaction of 4,5,6-triphenyl-1,2,3-triazine, which is an isomer of <B>1</B>, undergoes reductive N–N bond cleavage to give 3,4,5-triphenylpyrazole in good yield.
- 公益社団法人 日本化学会の論文
著者
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Nitta Makoto
Department Of Applied Pharmacology Toyama Medical And Pharmaceutical University
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Kobayashi Tomoshige
Department Of Chemistry Faculty Of Science Shinshu University
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Murata Naoki
Department Of Applied Chemistry Graduate School Of Engineering Osaka City University
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