![Late-stage peptide C–H alkylation for bioorthogonal C–H activation featuring solid phase peptide synthesis | Nature Communications Late-stage peptide C–H alkylation for bioorthogonal C–H activation featuring solid phase peptide synthesis | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-019-11395-3/MediaObjects/41467_2019_11395_Fig1_HTML.png)
Late-stage peptide C–H alkylation for bioorthogonal C–H activation featuring solid phase peptide synthesis | Nature Communications
Conotoxin analogues, and methods for synthesis of intramolecular dicarba bridge containing peptides - Patent 1984384
![Synthesis of Peptoids Containing Multiple Nhtrp and Ntrp Residues: A Comparative Study of Resin, Cleavage Conditions and Submonomer Protection. - Abstract - Europe PMC Synthesis of Peptoids Containing Multiple Nhtrp and Ntrp Residues: A Comparative Study of Resin, Cleavage Conditions and Submonomer Protection. - Abstract - Europe PMC](https://europepmc.org/articles/PMC7201050/bin/fchem-08-00370-g0005.jpg)
Synthesis of Peptoids Containing Multiple Nhtrp and Ntrp Residues: A Comparative Study of Resin, Cleavage Conditions and Submonomer Protection. - Abstract - Europe PMC
![Frontiers | Recent Progress in the Chemical Synthesis of Class II and S-Glycosylated Bacteriocins | Microbiology Frontiers | Recent Progress in the Chemical Synthesis of Class II and S-Glycosylated Bacteriocins | Microbiology](https://www.frontiersin.org/files/MyHome%20Article%20Library/311542/311542_Thumb_400.jpg)
Frontiers | Recent Progress in the Chemical Synthesis of Class II and S-Glycosylated Bacteriocins | Microbiology
![Greening the synthesis of peptide therapeutics: an industrial perspective - RSC Advances (RSC Publishing) DOI:10.1039/D0RA07204D Greening the synthesis of peptide therapeutics: an industrial perspective - RSC Advances (RSC Publishing) DOI:10.1039/D0RA07204D](https://pubs.rsc.org/image/article/2020/RA/d0ra07204d/d0ra07204d-f8_hi-res.gif)
Greening the synthesis of peptide therapeutics: an industrial perspective - RSC Advances (RSC Publishing) DOI:10.1039/D0RA07204D
![A general solid phase method for the synthesis of depsipeptides - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB26893K A general solid phase method for the synthesis of depsipeptides - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB26893K](https://pubs.rsc.org/image/article/2013/OB/c2ob26893k/c2ob26893k-s2.gif)
A general solid phase method for the synthesis of depsipeptides - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB26893K
![Selective Bi‐directional Amide Bond Cleavage of N‐Methylcysteinyl Peptide - Qiu - 2014 - European Journal of Organic Chemistry - Wiley Online Library Selective Bi‐directional Amide Bond Cleavage of N‐Methylcysteinyl Peptide - Qiu - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/50a90c84-4d3e-4f62-b568-4085142a2a1d/mfig000.jpg)