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通过N→S酰基转移将天然化学连接转变为反向反应。

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

作者信息

Macmillan Derek, Adams Anna, Premdjee Bhavesh

机构信息

Christopher Ingold Laboratories, Department of Chemistry, University College London 20 Gordon Street, London WC1H 0AJ, UK phone: +44 (0)20 7679 4684 e-mail:

出版信息

Isr J Chem. 2011 Nov;51(8-9):885-899. doi: 10.1002/ijch.201100084. Epub 2011 Oct 5.

Abstract

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.

摘要

全世界许多研究小组都在深入探索通过N→S酰基转移合成肽硫酯。这样做的原因可能包括使用基于Fmoc的化学方法进行前体组装的通常直接的方法以及本质上有趣的酰基迁移过程。在这篇综述中,我们介绍了这个令人兴奋的领域的最新进展,并更详细地讨论了我们自己通过在天然肽序列中进行N→S酰基转移来合成肽硫酯的努力。我们发现可以很容易地制备几种肽硫酯,而且,似乎有充分的进一步发展和发现的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc8e/3277902/89129774b9c8/ijch0051-0885-f4.jpg

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