Literature DB >> 23233036

Rapid formal hydrolysis of peptide-αthioesters.

Zachary P Gates1, Jules R Stephan, Dong Jun Lee, Stephen B H Kent.   

Abstract

In the presence of 2-mercaptoethanol peptide-(α)thioesters undergo smooth conversion to their corresponding peptide-(α)carboxylates. This general and operationally simple reaction extends the utility of a promising new strategy for cleaving resin-bound Boc/benzyl-protected peptides without the use of hydrogen fluoride.

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Year:  2013        PMID: 23233036     DOI: 10.1039/c2cc38229f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  9 in total

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Authors:  Andrew G Cheetham; Yu-Chuan Ou; Pengcheng Zhang; Honggang Cui
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4.  Development of a Chemical Methodology for the Preparation of Peptide Thioesters Applicable to Naturally Occurring Peptides Using a Sequential Quadruple Acyl Transfer System.

Authors:  Yusuke Tsuda; Akira Shigenaga; Kohei Tsuji; Masaya Denda; Kohei Sato; Keisuke Kitakaze; Takahiro Nakamura; Tsubasa Inokuma; Kohji Itoh; Akira Otaka
Journal:  ChemistryOpen       Date:  2015-04-28       Impact factor: 2.911

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Authors:  Sungjin Park; David T Krist; Alexander V Statsyuk
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7.  High-affinity free ubiquitin sensors for quantifying ubiquitin homeostasis and deubiquitination.

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Journal:  Nat Methods       Date:  2019-07-15       Impact factor: 28.547

8.  HF-Free Boc Synthesis of Peptide Thioesters for Ligation and Cyclization.

Authors:  Richard Raz; Fabienne Burlina; Mohamed Ismail; Julian Downward; Jiejin Li; Stephen J Smerdon; Martin Quibell; Peter D White; John Offer
Journal:  Angew Chem Int Ed Engl       Date:  2016-10-10       Impact factor: 15.336

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Journal:  J Pept Sci       Date:  2018-10-22       Impact factor: 1.905

  9 in total

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