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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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WILEY-VCH Verlag
2011
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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. |
format | Online Article Text |
id | pubmed-3277902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
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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