Chemoselective fragment condensation between peptide and peptidomimetic oligomers
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 11, Issue: 25, Page: 4142-4146
2013
- 16Citations
- 25Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations16
- Citation Indexes16
- 16
- CrossRef15
- Captures25
- Readers25
- 25
Article Description
We report the first example of chemoselective fragment condensation, through native amide bond formation, between peptoid and peptide oligomers. Peptoid oligomers bearing C-terminal salicylaldehyde esters were synthesized and ligated to peptides containing N-terminal serine or threonine residues. We investigate the ligation efficiency of peptoid oligomers varying in length, sequence, and C-terminal steric bulk. These protocols enhance accessibility of structurally complex peptoid-peptide hybrids and will facilitate the design new semi-synthetic proteins with unique attributes. © 2013 The Royal Society of Chemistry.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84878781958&origin=inward; http://dx.doi.org/10.1039/c3ob40606g; http://www.ncbi.nlm.nih.gov/pubmed/23715215; https://xlink.rsc.org/?DOI=c3ob40606g; https://dx.doi.org/10.1039/c3ob40606g; https://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob40606g
Royal Society of Chemistry (RSC)
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