Reactivity of 2-Methylene-1, 3-dicarbonyl Compounds. 1, 3-Dipolar Cycloaddition Reaction with Ethyl Diazoacetate

スポンサーリンク

概要

• 論文の詳細を見る

• The reaction of 2-methylene-1, 3-dicarbonyl compounds(1)with ethyl diazoacetate gave 4, 5-dihydro-1H-pyrazole derivatives(2), which were stable for several months at room temperature in good yields.

• 公益社団法人日本薬学会の論文
• 2001-12-01

著者

• Yamauchi M

  Josai Univ. Saitama Jpn

• Yamauchi Masashige

  Faculty Of Pharmaceutical Science Josai University

• YAJIMA Masahiko

  Faculty of pharmaceutical Sciences, Josai University

• Yajima M

  Faculty Of Pharmaceutical Sciences Josai University

関連論文

• Diastereoselective synthesis of 2-alkylated 4-silyloxyprolineesters
• The Influence of Ligand Side Chain on the Enantioselectivity of Lewis Acid Catalyzed Diels-Alder Reactions
• Synthesis of 1-Hydroxybicyclo[3.2.1]oct-3-en-2-ones by Acyloin Rearrangement of 1-Methoxy- or 1-tert-Butyldimethylsilyloxy-bicyclo[2.2.2]oct-5-en-2-ones
• Reactivity of 2-Methylene-1, 3-dicarbonyl Compounds. 1, 3-Dipolar Cycloaddition Reaction with Ethyl Diazoacetate
• Base-promoted Acyloin Rearrangement of 1,8-Di-tert-butyldimethylsilyl-oxybicyclo[2.2.2]oct-5-en-2-ones
• Photochemical Synthesis of Bicyclo[4.1.0]hept-2-enes

スポンサーリンク