PB90 STEREOSELECTIVE REDUCTION OF BICYCLIC KETALS : AN EFFICIENT ENTRY TO MEDIUM- AND LARGE-SIZED OXOCANE DERIVATIVES

スポンサーリンク

概要

• 論文の詳細を見る
• 天然有機化合物討論会の論文
• 1988-05-29

著者

• Ochi Masamitsu

  Department Of Chemistry Faculty Of Science Kochi University

• Kadota Isao

  Department Of Chemistry Faculty Of Science Kochi University

• Kotsuki Hiyoshizo

  Department Of Chemistry Faculty Of Science Kochi University

• Ushio Yasuyuki

  Department of Chemistry, Faculty of Science, Kochi University

• Ushio Yasuyuki

  Department Of Chemistry Faculty Of Science Kochi University

関連論文

• P-154 TOTAL SYNTHESIS OF BREVETOXIN B
• A New Enantioselective Synthesis of Aminodihydroisocoumarin Moiety of AI-77-B
• Organic Synthesis at High Pressure. Efficient Ring Opening Reaction of Epoxides with Heterocycles
• High-Pressure Promoted and Silica Gel Catalyzed Aminolysis of Epoxides with Glycine Esters
• P-82 A New Rapid Synthesis of Stentorin-C
• PB90 STEREOSELECTIVE REDUCTION OF BICYCLIC KETALS : AN EFFICIENT ENTRY TO MEDIUM- AND LARGE-SIZED OXOCANE DERIVATIVES
• P-140 Synthesis of the IJK Ring Segment of Yessotoxin
• P-141 Convergent Synthesis of Hemibrevetoxin B
• Synthesis of lateral root-inducing compounds using an efficient coupling reaction of chiral triflates.
• High pressure organic chemistry. V. Diels-Alder reactions of furan with acrylic and maleic esters.

スポンサーリンク