Literature DB >> 25166929

A photolabile linker for the solid-phase synthesis of peptide hydrazides and heterocycles.

Katrine Qvortrup1, Vitaly V Komnatnyy, Thomas E Nielsen.   

Abstract

A photolabile hydrazine linker for the solid-phase synthesis of peptide hydrazides and hydrazine-derived heterocycles is presented. The developed protocols enable the efficient synthesis of structurally diverse peptide hydrazides derived from the standard amino acids, including those with side-chain protected residues at the C-terminal of the resulting peptide hydrazide, and are useful for the synthesis of dihydropyrano[2,3-c]pyrazoles. The linker is compatible with most commonly used coupling reagents and protecting groups for solid-phase peptide synthesis.

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Year:  2014        PMID: 25166929     DOI: 10.1021/ol502219s

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


  3 in total

Review 1.  Oximes and Hydrazones in Bioconjugation: Mechanism and Catalysis.

Authors:  Dominik K Kölmel; Eric T Kool
Journal:  Chem Rev       Date:  2017-06-22       Impact factor: 60.622

2.  Exploiting the MeDbz Linker To Generate Protected or Unprotected C-Terminally Modified Peptides.

Authors:  Christine A Arbour; Hasina Y Saraha; Timothy F McMillan; Jennifer L Stockdill
Journal:  Chemistry       Date:  2017-08-15       Impact factor: 5.236

3.  Synthesis and biological evaluation of dihydropyrano-[2,3-c]pyrazoles as a new class of PPARγ partial agonists.

Authors:  Katrine Qvortrup; Jakob F Jensen; Mikael S Sørensen; Irene Kouskoumvekaki; Rasmus K Petersen; Olivier Taboureau; Karsten Kristiansen; Thomas E Nielsen
Journal:  PLoS One       Date:  2017-02-28       Impact factor: 3.240

  3 in total

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