Results 21 to 30 of about 414,318 (301)
Parallel solid-phase synthesis of diaryltriazoles
A series of substituted diaryltriazoles was prepared by a solid-phase-synthesis protocol using a modified Wang resin. The copper(I)- or ruthenium(II)-catalyzed 1,3-cycloaddition on the polymer bead allowed a rapid synthesis of the target compounds in a ...
Matthias Wrobel +2 more
doaj +1 more source
The solid-phase synthesis of the first example of a new diphosphate AICAR derivative is reported. The new substance is characterized by the presence of a 5'-phosphate group while a second phosphate moiety is installed on a 5-hydroxypentyl chain attached ...
Gennaro Piccialli +7 more
doaj +1 more source
Photolabile Linkers for Solid-Phase Synthesis [PDF]
Photolabile linkers are the subjects of intense research because they allow the release of the target molecule simply by irradiation. Photochemical release of synthesis products is often facilitated without additional reagents under mild reaction conditions, which may even be environmentally friendly and appealing in the context of greener chemistry ...
Remi J. T. Mikkelsen +4 more
openaire +5 more sources
Solid-Phase Synthesis of Substituted Tetramic Acids
Solid-Phase Synthesis of Substituted Tetramic ...
Jay Matthews (3040941) +1 more
core +2 more sources
New Solid Phase Synthesis of Distamycin Analogues
A novel and straightforward solid phase synthesis of distamycin analogues containing benzene units has been developed.
Drozdowska Danuta
doaj +1 more source
Rhodiasolv PolarClean – a greener alternative in solid-phase peptide synthesis
PolarClean, a green solvent prepared through the valorization of a byproduct of Nylon-66 manufacturing, shows an excellent capacity to dissolve all Fmoc-amino acids and key coupling reagents and additives.
Ashish Kumar +3 more
doaj +1 more source
Solid-Phase Total Synthesis of Plusbacin A3
The total synthesis of the depsipeptide natural product plusbacin A3 (1) utilizing solid-phase peptide synthesis (SPPS) was disclosed. A 3-hydroxy-proline derivative compatible with Fmoc SPPS was prepared by a diastereoselective Joullié–Ugi three ...
Toyotaka Sato +17 more
core +1 more source
Solid-Phase Synthesis of ?-Oligopeptides
Fmoc-N-Protected ?-amino acids of (S)-configuration bearing the side chains of Ala, Val, Leu, and Phe in the 3- and 2-position have been prepared. Manual solid-phase synthesis (ortho-chlorotrityl-chloride resin) of the ?-heptapeptides H-?3-HVal-?
Gilles Guichard, Dieter Seebach
doaj +2 more sources
Solid-Phase Unnatural Peptide Synthesis (UPS)
Solid-Phase Unnatural Peptide Synthesis ...
Martin J. O'Donnell (2489491) +2 more
core +2 more sources
Dendritic structures, being highly homogeneous and symmetric, represent ideal scaffolds for the multimerization of bioactive molecules and thus enable the synthesis of compounds of high valency which are e.g., applicable in radiolabeled form as ...
Gabriel Fischer +2 more
doaj +1 more source

