Synthesis of 3-0-Benzylstentorin Analog as Precursor for the Basic Skeleton of Blepharismin

Authors

  • TENI ERNAWATI LEMBAGA ILMU PENGETAHUAN INDONESIA ,
  • YOSHINOSUKE USUKI FACULTY OF SCIENCE OSAKA CITY UNIVERSITY ,
  • HIDEO IIO FACULTY OF SCIENCE OSAKA CITY UNIVERSITY ,

Keywords:

blepharismin, 3-0-benzylstentorin, synthesis, dimerization, anthraquinone derivative

Abstract

A Method for the synthesis of precursor for the basic skeleton of blepharismin and structural analog was described. Such compound is identified as potential drug for the treatment of antiviral and photodynamic therapy. Benzyl stentorin analog as the basic skeleton of blepharismin was effectively synthesized via reaction one of hydroxyl groups in bianthraquinone derivative with p-methoxybenzylchloride in the presence of potassium carbonate as base. Dimerization of bromo anthraquinone derivative produced dimmer in 55% while the formation of compounds analogous of 3-0-benzylstentorin resulted in 70% yield.

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Published

2012-04-30

Issue

Vol. 10 No. 1 (2012): JIFI

Section

Articles

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