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An improved preparation of 3-alkoxypyrazoles.

  作者 Guillou, Sandrine;Bonhomme, Frederic J.;Janin, Yves L.;  
  选自 期刊  Synthesis;  卷期  2008年-21;  页码  3504-3508  
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[摘要]The condensation between alkyl acetoacetates and hydrazines constitutes the very well-known Knorr synthetic method leading to pyrazol-3/5-ones. However, contemporary reports describe an alternate reaction pathway leading to low yields of 3/5-alkoxypyrazoles using hydrazine salts. No general method for the selective synthesis of 3-alkoxypyrazoles was reported to date, hence the authors focused on this side reaction in an attempt to turn it into the main transformation. Depending on the starting material, various 3-alkoxypyrazoles (methoxy, ethoxy, benzyloxy, isopropoxy, allyloxy) were obtained in ?6% yield.

 
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