Design and Synthesis of Cyclic RGD Pentapeptoids by Consecutive Ugi Reactions

A new strategy for the synthesis of cyclic peptoids was developed. The approach is based on the use of consecutive Ugi reactions for the assembly of the acyclic peptoid and for the ring closure. Cyclopentapeptoid analogues of the RGD peptides were designed and synthesized using this methodology. The...

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Veröffentlicht in:Organic letters 2008-01, Vol.10 (2), p.205-208
Hauptverfasser: Vercillo, Otilie E, Andrade, Carlos Kleber Z, Wessjohann, Ludger A
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creator Vercillo, Otilie E
Andrade, Carlos Kleber Z
Wessjohann, Ludger A
description A new strategy for the synthesis of cyclic peptoids was developed. The approach is based on the use of consecutive Ugi reactions for the assembly of the acyclic peptoid and for the ring closure. Cyclopentapeptoid analogues of the RGD peptides were designed and synthesized using this methodology. The results confirm the versatility and efficiency of the method for the preparation of cyclic oligopeptoids.
doi_str_mv 10.1021/ol702521g
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subjects Cyclization
Models, Molecular
Molecular Structure
Peptides, Cyclic - chemical synthesis
Peptides, Cyclic - chemistry
Peptoids - chemical synthesis
Peptoids - chemistry
title Design and Synthesis of Cyclic RGD Pentapeptoids by Consecutive Ugi Reactions
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