Literature DB >> 23075145

Trimethoxyphenylthio as a highly labile replacement for tert-butylthio cysteine protection in Fmoc solid phase synthesis.

Tobias M Postma1, Matthieu Giraud, Fernando Albericio.   

Abstract

Trimethoxyphenylthio (S-Tmp) is described as a novel cysteine protecting group in Fmoc solid phase peptide synthesis replacing the difficult to remove tert-butylthio. S-Tmp and dimethoxyphenylthio (S-Dmp) were successfully used for cysteine protection in a variety of peptides. Moreover, both groups can be removed in 5 min with mild reducing agents. S-Tmp is recommended for cysteine protection, as it yields crude peptides of high purity.

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Year:  2012        PMID: 23075145     DOI: 10.1021/ol3025499

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  9 in total

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Journal:  Biochemistry       Date:  2018-03-06       Impact factor: 3.162

5.  Rapid analysis of protein farnesyltransferase substrate specificity using peptide libraries and isoprenoid diphosphate analogues.

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Authors:  Sam J Moons; Rens A Mensink; Jeroen P J Bruekers; Maurits L A Vercammen; Laura M Jansen; Thomas J Boltje
Journal:  J Org Chem       Date:  2019-03-07       Impact factor: 4.354

8.  Immobilized N-chlorosuccinimide as a friendly peptide disulfide-forming reagent.

Authors:  Tobias M Postma; Fernando Albericio
Journal:  ACS Comb Sci       Date:  2014-03-31       Impact factor: 3.784

9.  Understanding acid lability of cysteine protecting groups.

Authors:  Iván Ramos-Tomillero; Lorena Mendive-Tapia; Miriam Góngora-Benítez; Ernesto Nicolás; Judit Tulla-Puche; Fernando Albericio
Journal:  Molecules       Date:  2013-05-06       Impact factor: 4.411

  9 in total

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