Stereoselective Bifurcating-type Radical Cyclization of gem-Dibromocyclopropanes for the Synthesis of Uniquely Fused 5-3-5-Type Tricyclic Compounds

スポンサーリンク

概要

• 論文の詳細を見る
• 2002-01-05

著者

• Tanabe Yoo

  School Of Science Kwansei Gakuen University

• Yanagi Kazunori

  Environmental Health Science Laboratory Sumitomo Chemical Co. Ltd.

• Wakasugi Kazunori

  School Of Science Kwansei Gakuin University

• Nishii Yoshinori

  The Physical Chemical Research Institute (riken)

• FUJIWARA Atsushi

  School of Science, Kwansei Gakuin University

• MIKI Misao

  Environmental Health Science Laboratory, Sumitomo Chemical Co. Ltd.

• Miki Misao

  Environmental Health Science Laboratory Sumitomo Chemical Co. Ltd.

• Fujiwara Atsushi

  School Of Science Kwansei Gakuin University

関連論文

• Synthesis and Fungicidal Activity of 1- (α-tert-Butylcinnamoyl) imidazoles(Organic Chemistry)
• 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

スポンサーリンク