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Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer

Peptide thioester synthesis by N→S acyl transfer is being intensively explored by many research groups the world over. Reasons for this likely include the often straightforward method of precursor assembly using Fmoc-based chemistry and the fundamentally interesting acyl migration process. In this r...

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Detalles Bibliográficos
Autores principales: Macmillan, Derek, Adams, Anna, Premdjee, Bhavesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277902/
https://www.ncbi.nlm.nih.gov/pubmed/22347724
http://dx.doi.org/10.1002/ijch.201100084
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author Macmillan, Derek
Adams, Anna
Premdjee, Bhavesh
author_facet Macmillan, Derek
Adams, Anna
Premdjee, Bhavesh
author_sort Macmillan, Derek
collection PubMed
description Peptide thioester synthesis by N→S acyl transfer is being intensively explored by many research groups the world over. Reasons for this likely include the often straightforward method of precursor assembly using Fmoc-based chemistry and the fundamentally interesting acyl migration process. In this review we introduce recent advances in this exciting area and discuss, in more detail, our own efforts towards the synthesis of peptide thioesters through N→S acyl transfer in native peptide sequences. We have found that several peptide thioesters can be readily prepared and, what’s more, there appears to be ample opportunity for further development and discovery.
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spelling pubmed-32779022012-02-15 Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer Macmillan, Derek Adams, Anna Premdjee, Bhavesh Isr J Chem Reviews Peptide thioester synthesis by N→S acyl transfer is being intensively explored by many research groups the world over. Reasons for this likely include the often straightforward method of precursor assembly using Fmoc-based chemistry and the fundamentally interesting acyl migration process. In this review we introduce recent advances in this exciting area and discuss, in more detail, our own efforts towards the synthesis of peptide thioesters through N→S acyl transfer in native peptide sequences. We have found that several peptide thioesters can be readily prepared and, what’s more, there appears to be ample opportunity for further development and discovery. WILEY-VCH Verlag 2011-11 2011-10-05 /pmc/articles/PMC3277902/ /pubmed/22347724 http://dx.doi.org/10.1002/ijch.201100084 Text en Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Reviews
Macmillan, Derek
Adams, Anna
Premdjee, Bhavesh
Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title_full Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title_fullStr Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title_full_unstemmed Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title_short Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
title_sort shifting native chemical ligation into reverse through n→s acyl transfer
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277902/
https://www.ncbi.nlm.nih.gov/pubmed/22347724
http://dx.doi.org/10.1002/ijch.201100084
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