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Cyclisation of histidine containing peptides in the solid-phase by anchoring the imidazole ring to trityl resins

✍ Scribed by Giuseppina Sabatino; Mario Chelli; Silvia Mazzucco; Mauro Ginanneschi; Anna Maria Papini


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
284 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


Head-to-tail histidine containing cyclopeptides can be efficiently synthesised by a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/allyl) v/a anchoring the imidazole ring to trityi-resins. Furthermore, Fmoc-His(Trt-®)-OAl can be a useful starting support for the preparation of diketopiperazine combinatorial libraries.