Fig. 6 | Nature Communications

Fig. 6

From: Direct and efficient synthesis of nucleosides through the ortho-(tert-butylethynyl)phenyl thioglycosides (BEPTs) protocol

Fig. 6

Synthesis of 2′-deoxynucleoside derivatives by the combination of BEPT protocol and photocatalyzed C–O bond editing techniques (1,4-dihydroisonicotinoyl (DHIN) was used as a stereo-controlling and deoxygenation-initiating group, and the direct saturation of the DHIN group to isonicotinoyl (IN) group was found to be the major side reaction).

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