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Design and Effective Synthesis of the First 4-Aza-2,3-didehydropodophyllotoxin Rigid Aminologue: A N-Methyl-4-[(3,4,5-trimethoxyphenyl)amino)]-1,2-dihydroquinoline-lacton e.

  作者 Labruere, Raphael;Helissey, Philippe;Desbene-Finck, Stephanie;Giorgi-Renault, Sylviane;  
  选自 期刊  Journal of Organic Chemistry;  卷期  2008年73-9;  页码  3642-3645  
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[摘要]The first N1-alkyl-4-amino-1,2-dihydroquinoline-lactone I has been prepd. by a five-step sequence in a 51% overall yield via the corresponding furo[3,4-b]quinolin-1(3H)-one. A new practical synthesis of this intermediate was carried out using versatile, com. available starting materials and constitutes the shortest and highest yielding route. These synthetic pathways could be widened with a view toward the prepn. of different substituted derivs., which could be considered as rigid aminologues of 4-aza-2,3-didehydropodophyllotoxins.

 
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