Literature DB >> 15575761

Pseudoprolines as removable turn inducers: tools for the cyclization of small peptides.

Danielle Skropeta1, Katrina A Jolliffe, Peter Turner.   

Abstract

The cyclization of small peptides which do not incorporate turn inducers is often difficult. We have developed a method involving the use of removable turn inducers, in the form of pseudoprolines, for the cyclization of difficult peptide sequences. The pseudoprolines induce a cisoid amide bond in the peptide backbone which facilitates cyclization. They are then readily removed to yield a cyclic peptide that does not contain any turn inducers.

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Year:  2004        PMID: 15575761     DOI: 10.1021/jo0484732

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  12 in total

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Review 9.  Recent Reports of Solid-Phase Cyclohexapeptide Synthesis and Applications.

Authors:  Allan M Prior; Taylor Hori; Ashriel Fishman; Dianqing Sun
Journal:  Molecules       Date:  2018-06-18       Impact factor: 4.411

10.  A Chemical Biology Approach to Understanding Molecular Recognition of Lipid II by Nisin(1-12): Synthesis and NMR Ensemble Analysis of Nisin(1-12) and Analogues.

Authors:  Rachael Dickman; Emma Danelius; Serena A Mitchell; D Flemming Hansen; Máté Erdélyi; Alethea B Tabor
Journal:  Chemistry       Date:  2019-10-10       Impact factor: 5.236

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