Replace tBu with THP or Trt and give your amino acids a smarter protection, removable under milder acidic conditions to minimize side products. Learn more in our latest publication!
Optimize your drug delivery with non-immunogenic biodegradable PEG alternatives and discover strategies for synthesizing defined sarcosine oligomers for targeted drug conjugation.
Polysarcosines are flexible and enzyme-resistant polymers, made from the biocompatible non-proteinogenic amino acid sarcosine. Unlike PEGs, they are not reported to trigger immune responses.
Discover a greener synthetic approach towards peptide hydrazides - valuable precursors, e.g., for the synthesis of peptide thioesters, widely applied building blocks for native chemical ligation.
Amino-Li resin – a cross-linked polyacrylic amide solid support suitable for the synthesis of peptides and biomolecules, which is compatible with organic as well as aqueous solvents.
Herein we investigate the incorporation of the Fmoc-Thr-pseudoproline monomer during Fmoc SPPS. Typically, pseudoprolines are incorporated as preformed dipeptides. However, the possibility of using the monomer adds flexibility to the synthesis.
As the molecular diversity of cyclic and branched peptides becomes more and more challenging, a high level of orthogonal dimensionality is required. Herein, we present a new category of orthogonal protecting groups.
Herein, we report the first-time SPPS of a special peptide sequence via employment of of a serine pseudoproline building block as well as sec-isamyl mercaptan (SIT) as cysteine protecting group.
Common protocols for the loading of 2-CTC and MBH-Br resins presume the application of DCM, THF, or DMF; these solvents are considered as undesirable in accordance with modern regulatory rules.