The [4+2] Cycloaddition of 1,6-Dihydro-2-dimethylamino-4,6,6-trimethylpyrimidine with Acetylenic Compounds(Organic,Chemical)
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概要
- 論文の詳細を見る
1,6-Dihydro-2-dimethylamino-4,6,6-trimethylpyrimidine reacted with acetylenic compounds containing electron-withdrawing groups to yield 2-dimethylaminopyridine derivatives. When monosubstituted acetylenes were used, 4-unsubstituted pyridines were selectively obtained. The results of MINDO/3 calculations are consistent with this regioselectivity.
- 公益社団法人日本薬学会の論文
- 1987-07-25
著者
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鹿島 長次
Department of Chemistry, University of Tsukuba
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表 美守
Department Of Chemistry University Of Tsukuba
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清水 政男
Department Of Chemistry University Of Tsukuba
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鹿島 長次
筑波大学化学系
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鹿島 長次
Department Of Chemistry University Of Tsukuba
関連論文
- Studies on 1-(2-Phenethyl)-4-(N-propionylanilino)piperidine (Fentanyl) and Related Compounds. I. Spectrometric and Chromatographic Analyses of 3-Methylfentanyl and α-Methylfentanyl
- Dimroth-Type Ring Transformation of 1,4,6-Trisubstituted-2 (1H)-Pyrimidinethiones with Ammonia and Primary Alkyl Amines
- Ring Transformation Reaction of 1,4,6-Trisubstituted 2 (1H)-Pyrimidinones and -Thiones with Hydroxylamine
- Ring Transformation Reactions of 1-Substituted 2 (1H)-Pyrimidinones and Related Compounds with Active Methylene Compounds
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- The [4+2] Cycloaddition of 1,6-Dihydro-2-dimethylamino-4,6,6-trimethylpyrimidine with Acetylenic Compounds(Organic,Chemical)
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