Comparative evaluation of four trityl-type amidomethyl polystyrene resins in Fmoc solid phase peptide synthesis

2003 ◽  
Vol 9 (7) ◽  
pp. 419-429 ◽  
Author(s):  
Christos Zikos ◽  
Evangelia Livaniou ◽  
Leondios Leondiadis ◽  
Nikolas Ferderigos ◽  
Dionyssis S. Ithakissios ◽  
...  
Keyword(s):  
Peptide Synthesis ◽  
Comparative Evaluation ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Polystyrene Resins

ReGreen SPPS: enabling circular chemistry in environmentally sensible solid-phase peptide synthesis

2019 ◽  
Vol 21 (21) ◽  
pp. 5990-5998 ◽  
Author(s):  
Jan Pawlas ◽  
Jon H. Rasmussen
Keyword(s):  
Peptide Synthesis ◽  
Efficient Method ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Polystyrene Resins

A cost and synthetic efficient method that enables facile reagent and solvent recycling in SPPS using cross-linked polystyrene resins in greener solvents is reported.

Polystyrene resins cross-linked with di- or tri(ethylene glycol) dimethacrylates as supports for solid-phase peptide synthesis

Tetrahedron ◽  
2006 ◽  
Vol 62 (20) ◽  
pp. 4948-4953 ◽  
Author(s):  
Yu Wang ◽  
Genghui Zhang ◽  
Husheng Yan ◽  
Yunge Fan ◽  
Zuoqing Shi ◽  
...  
Keyword(s):  
Ethylene Glycol ◽  
Peptide Synthesis ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Polystyrene Resins

A Strategy for Thioamide Incorporation During Fmoc Solid-Phase Peptide Synthesis with Robust Stereochemical Integrity

2019 ◽  
Author(s):  
luis camacho III ◽  
Bryan J. Lampkin ◽  
Brett VanVeller
Keyword(s):  
Amino Acid ◽  
Functional Groups ◽  
Peptide Synthesis ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Side Chains ◽  
Amino Acid Side Chains ◽  
Peptide Elongation

We describe a method to protect the sensitive stereochemistry of the thioamide—in analogy to the protection of the functional groups of amino acid side chains—in order to preserve the thioamide moiety during peptide elongation.<br>

Analytical Methods for Solid Phase Peptide Synthesis

2004 ◽  
Vol 8 (4) ◽  
pp. 291-301 ◽  
Author(s):  
Giuseppina Sabatino ◽  
Mario Chelli ◽  
Alberto Brandi ◽  
Anna Papini
Keyword(s):  
Peptide Synthesis ◽  
Analytical Methods ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis

Fmoc Solid Phase Peptide Synthesis

1999 ◽  
Keyword(s):  
Peptide Synthesis ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Peptide Chain ◽  
Standard Approach ◽  
Side Chain ◽  
Complex Structures ◽  
Protein Conjugation ◽  
Chemoselective Ligation ◽  
Routine Production

In the years since the publication of Atherton and Sheppard's volume, the technique of Fmoc solid-phase peptide synthesis has matured considerably and is now the standard approach for the routine production of peptides. The basic problems outstanding at the time of publication of this earlier work have now been, for the most part, solved. As a result, innovators in the field have focussed their efforts to develop methodologies and chemistry for the synthesis of more complex structures. The focus of this new volume is much broader, and covers not only the essential procedures for the production of linear peptides but also more advanced techniques for preparing cyclic, side-chain modified, phospho- and glycopeptides. Many other methods also deserving attention have been included: convergent peptide synthesis; peptide-protein conjugation; chemoselective ligation; and chemoselective purification. The difficult preparation of cysteine and methionine-containing peptides is also covered, as well as methods for overcoming aggregation during peptide chain assembly and a survey of available automated instrumentation.

scholarly journals Cover Picture: Propylphosphonic Anhydride (T3P®) as Coupling Reagent for Solid‐Phase Peptide Synthesis (11/2021)

2021 ◽  
Vol 6 (11) ◽  
pp. 2648-2648
Author(s):  
Othman Al Musaimi ◽  
Richard Wisdom ◽  
Peter Talbiersky ◽  
Beatriz G. De La Torre ◽  
Fernando Albericio
Keyword(s):  
Peptide Synthesis ◽  
Solid Phase ◽  
Solid Phase Peptide Synthesis ◽  
Coupling Reagent
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