A Simple One-Pot Synthesis of tert-Butyldimethylsilyl-Protected Cyanohydrins(Organic,Chemical)
スポンサーリンク
概要
- 論文の詳細を見る
A direct conversion of a variety of aldehydes to the corresponding terf-butyldimethylsilyl protected cyanohydrins is described, by using tert-butyldimethylsilyl chloride and lithium cyanide.
- 公益社団法人日本薬学会の論文
- 1987-09-25
著者
-
Kurihara T
Osaka University Of Pharmaceutical Sciences
-
HARUSAWA Shinya
Osaka University of Pharmaceutical Sciences
-
YONEDA Ryuji
Osaka University of Pharmaceutical Sciences
-
KURIHARA Takushi
Osaka University of Pharmaceutical Sciences
-
HISAKAWA HIDEKI
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 and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5-amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity
- Meisenheimer Rearrangement of Azetopyridoindoles. VIII. Synthesis and Antiviral Activities of 12-Carbaeudistomin Analogs
- Efficient Synthesis of trans- or cis-4(5)-(5-Aminomethyltetrahydrofuran-2-yl)imidazoles via Diazafulvene Intermediates: Synthetic Approach toward Human Histamine H_4-Ligands
- Studies on the [2,3]-Meisenheimer Rearrangement of 2-Vinylazetidine N-Oxides
- A Simple One-Pot Synthesis of tert-Butyldimethylsilyl-Protected Cyanohydrins(Organic,Chemical)