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Abstract This thesis includes three chapters; the first of which is a review of themethodsutilized for the synthesis of the various types of tetraseconucleosideass well as their biological activities. The second chapter contains two parts deal with the synthesis of dillereo; acyclic nucleosides mainly of the diseco- and tetraseconucleosidesr, espectively. Thus, reaction of the 2(1H)-quinoxalinone with 5-chloro-3-oxapentylacetate afforded 1-(5-acetoxy-3-oxapentyl)- 2( 1/1)- quinoxalinone(I) and 2-(5-acetoxy-3-oxapentyloxy)quinoxaline (ll), whose deprotection of the hydroxyl group gave 1-(5-hydroxy-3- oxapentyl)-2(1H)-quinoxalinone(llI) and 2-(5-hydroxy-3-oxapentyloxy)- quinoxalin(IeV), respectively. QN N V”o”””v ’>r--1 o QN N RO/”’-..../O~ o~ I R=Ac II R = Ac llR=H IV R=H |