Mild Approach to Nucleoside Analogues via Photoredox/Cu-Catalyzed Decarboxylative C-N Bond Formation. Total Synthesis
Ruonan Wang1,2, Hao Xu2, Arpan Banerjee2
1College of Chemistry and Henan Institute of Advanced Technology, Zhengzhou University, 100 Science Avenue, Zhengzhou 450001, China.
Abstract:
The conventional N-glycosylation methods for nucleoside synthesis usually require strongly acidic or basic conditions. Here we report the decarboxylative C(sp3)-N coupling of glycosyl N-hydroxyphthalimide esters with nucleobases via dual photoredox/Cu catalysis, which offered a mild approach to nucleoside analogues. A total synthesis of oxetanocin A, an antiviral natural product containing an oxetanose moiety, has been achieved by using this method.
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