Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology
The conversion of thioesters to amides via acyl transfer has become one of the most important synthetic techniques for the chemical synthesis and modification of proteins. This review discusses this S-to-N acyl transfer process, and highlights some of the key applications across chemistry and biolog...
Guardado en:
Autores principales: | , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/59417d48b6dc4b2da4db6f05832ae640 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:59417d48b6dc4b2da4db6f05832ae640 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:59417d48b6dc4b2da4db6f05832ae6402021-12-02T17:06:26ZExploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology10.1038/ncomms156552041-1723https://doaj.org/article/59417d48b6dc4b2da4db6f05832ae6402017-05-01T00:00:00Zhttps://doi.org/10.1038/ncomms15655https://doaj.org/toc/2041-1723The conversion of thioesters to amides via acyl transfer has become one of the most important synthetic techniques for the chemical synthesis and modification of proteins. This review discusses this S-to-N acyl transfer process, and highlights some of the key applications across chemistry and biology.Helen M. BurkeLauren McSweeneyEoin M. ScanlanNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-16 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Science Q |
spellingShingle |
Science Q Helen M. Burke Lauren McSweeney Eoin M. Scanlan Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
description |
The conversion of thioesters to amides via acyl transfer has become one of the most important synthetic techniques for the chemical synthesis and modification of proteins. This review discusses this S-to-N acyl transfer process, and highlights some of the key applications across chemistry and biology. |
format |
article |
author |
Helen M. Burke Lauren McSweeney Eoin M. Scanlan |
author_facet |
Helen M. Burke Lauren McSweeney Eoin M. Scanlan |
author_sort |
Helen M. Burke |
title |
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
title_short |
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
title_full |
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
title_fullStr |
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
title_full_unstemmed |
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology |
title_sort |
exploring chemoselective s-to-n acyl transfer reactions in synthesis and chemical biology |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/59417d48b6dc4b2da4db6f05832ae640 |
work_keys_str_mv |
AT helenmburke exploringchemoselectivestonacyltransferreactionsinsynthesisandchemicalbiology AT laurenmcsweeney exploringchemoselectivestonacyltransferreactionsinsynthesisandchemicalbiology AT eoinmscanlan exploringchemoselectivestonacyltransferreactionsinsynthesisandchemicalbiology |
_version_ |
1718381612854411264 |