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First aromatic electrophilic iodination reaction on the solid-phase: Iodination of bioactive peptides

✍ Scribed by Gemma Arsequell; Gemma Espuña; Gregorio Valencia; José Barluenga; Raquel Pérez Carlón; JoséM. González


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
251 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


Direct iodination of Tyr residues of peptides anchored on solid supports was accomplished, for the first time, by aromatic eleclrophilic attack of iodonium ions provided by the IPy2BF 4 reagent. Compatibility studies of the iodination with routine solid-phase synthesis protocols are reported.


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