Head-to-tail histidine containing cyclopeptides can be efficiently synthesised by a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/allyl) via anchoring the imidazole ring to trityl-resins. Furthermore, Fmoc-His(Trt-(R))-OAl can be a useful starting support for the preparation of diketopiperazine combinatorial libraries. (C) 1999 Elsevier Science Ltd. All rights reserved.
Cyclisation of histidine containing peptides in the solid-phase by anchoring the imidazole ring to trityl resins
Sabatino G;
1999
Abstract
Head-to-tail histidine containing cyclopeptides can be efficiently synthesised by a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/allyl) via anchoring the imidazole ring to trityl-resins. Furthermore, Fmoc-His(Trt-(R))-OAl can be a useful starting support for the preparation of diketopiperazine combinatorial libraries. (C) 1999 Elsevier Science Ltd. All rights reserved.File in questo prodotto:
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