Direct and Electrophilic Preparation of α-Thiocyanatoketones and Aldehydes Using Thiocyanatotrimethylsilane and Sulfuryl Chloride
スポンサーリンク
概要
- 論文の詳細を見る
- 1994-12-05
著者
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Tanabe Yoo
School Of Science Kwansei Gakuen University
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Mori Kei
School Of Science Kwansei Gakuin University
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MAKITA Takuya
School of Science, Kwansei Gakuin University
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Makita Takuya
School Of Science Kwansei Gakuin University
関連論文
- A Novel and Regioselective Radical Cyclization of gem-Dihalocyclopropyl Substituted Alkenes and Alkynes Using Tributyltin Hydride and Catalytic AIBN
- Highly Stereoselective Synthesis of the Anti-Platelet Activating Factor, 4-Thiazolidinones, Using Silyl Derivatives of 2-Mercaptoalkanoic Acids
- Practical and Safe Sulfonylation of 2-Alkynyl and 2-Alkenyl Alcohols Using the Combined Bases of a Catalytic Amount of Tertiary Amine and Potassium Carbonate
- Stereoselective Bifurcating-type Radical Cyclization of gem-Dibromocyclopropanes for the Synthesis of Uniquely Fused 5-3-5-Type Tricyclic Compounds
- Direct and Electrophilic Preparation of α-Thiocyanatoketones and Aldehydes Using Thiocyanatotrimethylsilane and Sulfuryl Chloride
- Novel Synthetic Pyrethroid Containing a Halocyclopropane Structure
- First Total Synthesis of (±)-Podoblastins A-C, Natural Anti-rice-blast Fungicides, by Utilizing Novel Fries-type Acyl Rearrangement as a Key Step : Structure-activity Relationship of These Compounds and New Synthetic Analogs