166410-32-8Relevant articles and documents
Cotton functionalized with peptides: Characterization and synthetic methods
Orlandin, Andrea,Formaggio, Fernando,Toffoletti, Antonio,Peggion, Cristina
, p. 547 - 553 (2014)
Three approaches for the chemical ligation of peptides to cotton fibers are described and compared. This investigation was encouraged by the need to create peptide-decorated natural textiles, furnished with useful properties (e.g. antimicrobial activity). IR absorption spectroscopy is proved to be an easy and fast method to check the covalent anchorage of a peptide to cotton, whereas for a quantitative determination, a UV absorption method was employed. We also analyzed the usefulness of electron paramagnetic resonance spectroscopy to characterize our peptide-cotton conjugates. Copyright 2014 European Peptide Society and John Wiley & Sons, Ltd. In this work, three approaches for the chemical ligation of peptides and dendrimers to cotton fibers are described and compared. Characterization of the peptide bound to the cotton was achieved by means of IR absorption, UV, and electron paramagnetic resonance spectroscopies. Copyright
Maintaining homogeneity during a sol-gel transition by an autocatalytic enzyme reaction
Panja, Santanu,Adams, Dave J.
, p. 47 - 50 (2019)
Kinetic control over supramolecular gelation by increasing the pH can be achieved using an enzymatic reaction. This method allows us to produce homogeneous hydrogels with superior and improved mechanical properties as compared to gels obtained from simple addition of base.
Flow-mediated synthesis of Boc, Fmoc, and Dd iv monoprotected diamines
Jong, Thingsoon,Bradley, Mark
supporting information, p. 422 - 425 (2015/03/03)
A series of monoprotected aliphatic diamines (21 examples) were synthesized via continuous flow methods. The carbamates and enamines were obtained in 45-91% yields using a 0.5 mm diameter PTFE tubular flow reactor. Using readily accessible protecting group precursors, the procedure serves as an attractive alternative to existing batch-mode synthetic routes by providing direct, multigram access to N-Boc-, N-Fmoc-, and N-Ddiv-protected compounds with productivity indexes of 1.2-3.6 g/h.
