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- W2949986251 abstract "Heteroaromatic bases containing nitrogen atoms were easily alkylated with carboxylic acids in the presence of [bis(trifluoroacetoxy)iodo] benzene and [bis(trifluoroacetoxy)iodo]pentafluorobenzene via radical pathways. Similarly, the alkylation onto heteroaromatic bases was carried out with oxalic acid monoalkyl esters, which were prepared from alcohols and oxalyl dichloride, in the presence of the same trivalent iodine compounds. Moreover, this system was applied to the synthesis of C-nucleosides with the carboxylic acids bearing a sugar moiety." @default.
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- W2949986251 date "2010-08-19" @default.
- W2949986251 modified "2023-09-26" @default.
- W2949986251 title "ChemInform Abstract: Radical Decarboxylative Alkylation Onto Heteroaromatic Bases with Trivalent Iodine Compounds." @default.
- W2949986251 cites W2102229019 @default.
- W2949986251 doi "https://doi.org/10.1002/chin.199405106" @default.
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