Electrophilic substitution at C-5 in 1-methyl-5,6-dihydrocytosine
Abstract
1-Methyl-5,6-dihydrocytosine is rapidly deuteriated at C-5 at neutral pD's, treatment with iodine affords the 5-iodo-compound, and aminomethylation gives an unusual 5,5-disubstituted product (IV).
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