A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates1. Issue 62 (11th August 2015) - Xie, Ming-Sheng
Abstract A straightforward entry to chiral carbocyclic nucleoside analogues is achieved via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates to vinyl cyclopropanes.