
A variety of nucleic acids can be catalytically alkylated with rhodium-carbenoids generated from diazo compounds in aqueous buffer through an NH insertion process (see scheme; MES=2-(N-morpholino)ethanesulfonic acid). The method specifically targets unpaired bases such as those present in single strands, turn regions, and overhangs while leaving double-stranded sequences untouched.
Structure-Activity Relationship, Alkylation, Nucleic Acid Conformation, RNA, Rhodium, DNA, Catalysis, Substrate Specificity
Structure-Activity Relationship, Alkylation, Nucleic Acid Conformation, RNA, Rhodium, DNA, Catalysis, Substrate Specificity
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