Synthesis of Novel Nucleoside Analogues Built on a Bicyclo[4.1.0]heptane Scaffold
JOURNAL OF ORGANIC CHEMISTRY(2015)
摘要
A new class of carbocyclic nucleoside analogues built on a bicyclo [4.1.0]heptane scaffold, a perspective novel pseudosugar pattern, have been conceived as anti-HSV agents on the basis of initial protein ligand docking studies. The asymmetric synthesis of a series of these compounds incorporating different nucleobases has been efficiently completed starting from 1,4-cydohexanedione.
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