Stereoselective Synthesis of 4(5)-[(2S,3S)- and (2R,3R)-3-Aminotetrahydrofuran-2-yl)imidazoles Using Modified and Standard Mitsunobu Cyclizations: Synthetic Studies toward Novel Histamine H3-Ligands
スポンサーリンク
概要
著者
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ARAKI Lisa
Osaka University of Pharmaceutical Sciences
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Araki L
Osaka University Of Pharmaceutical Sciences
関連論文
- Synthesis of Novel 4(5)-(5-Aminotetrahydropyran-2-yl)imidazole Derivatives and Their in Vivo Release of Neuronal Histamine Measured by Brain Microdialysis
- Synthesis of (±)-trans- or cis-(5-Aminomethyltetrahydrofuranyl)imidazole by Mitsunobu Cyclization : Synthetic Studies toward Novel Histamine H_3 or H_4-Ligands
- Efficient Synthesis of trans- or cis-4(5)-(5-Aminomethyltetrahydrofuran-2-yl)imidazoles via Diazafulvene Intermediates: Synthetic Approach toward Human Histamine H_4-Ligands
- Synthesis of cis- or trans-2,4-Disubstituted Tetrahydrofurans Bearing Amino and Imidazole Groups by Efficient Use of the Modified or Standard Mitsunobu Cyclization: Synthetic Studies toward Novel Histamine H3-Ligands
- Stereoselective Synthesis of 4(5)-[(2S,3S)- and (2R,3R)-3-Aminotetrahydrofuran-2-yl)imidazoles Using Modified and Standard Mitsunobu Cyclizations: Synthetic Studies toward Novel Histamine H3-Ligands
- Studies on the [2,3]-Meisenheimer Rearrangement of 2-Vinylazetidine N-Oxides