scholarly journals Correction: Borinic acid catalysed peptide synthesis

2018 ◽  
Vol 54 (40) ◽  
pp. 5142-5142 ◽  
Author(s):  
Tharwat Mohy El Dine ◽  
Jacques Rouden ◽  
Jérôme Blanchet
Keyword(s):  
Peptide Synthesis ◽  
Borinic Acid

Correction for ‘Borinic acid catalysed peptide synthesis’ by Tharwat Mohy El Dine et al., Chem. Commun., 2015, 51, 16084–16087.

scholarly journals Borinic acid catalysed peptide synthesis

2015 ◽  
Vol 51 (89) ◽  
pp. 16084-16087 ◽  
Author(s):  
Tharwat Mohy El Dine ◽  
Jacques Rouden ◽  
Jérôme Blanchet
Keyword(s):  
Peptide Synthesis ◽  
Molecular Sieves ◽  
Borinic Acid

2-Chlorophenylborinic acid is reported to catalyze dipeptide synthesis in the presence of molecular sieves with no racemization.

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

Peptide Synthesis

BIO-PROTOCOL ◽  
2012 ◽  
Vol 2 (14) ◽  
Author(s):  
Zheng Miao ◽  
Zhen Cheng
Keyword(s):  
Peptide Synthesis

Series of sequential polypeptides containing lysine or arginine: Preparation and characterization

1988 ◽  
Vol 53 (1) ◽  
pp. 145-156 ◽  
Author(s):  
Jana Pírková ◽  
Svetlana Churkina ◽  
Vladimír Gut ◽  
Ivo Frič ◽  
Karel Bláha
Keyword(s):  
Molecular Weight ◽  
Amino Acid ◽  
Peptide Synthesis ◽  
Average Molecular Weight ◽  
Basic Amino Acid ◽  
Cd Spectra ◽  
Active Esters ◽  
Marked Tendency

The sequential polypeptides (Lys-Ala)n, (Lys-Ala-Ala)n, (Lys-Ala-Ala-Ala)n, (Lys-Leu-Ala)n, (Lys-Leu-Ala-Ala)n, (Lys-Leu-Ala-Ala-Ala)n, (Lys-Ala-Leu)n, (Lys-Ala-Leu-Ala)n, (Orn-Leu-Ala)n,(Arg-Ala-Ala)n, (Arg-Leu-Ala)n, (Arg-Leu-Ala-Ala)n, (Arg-Ala-Leu)n, and (Arg-Ala-Leu-Ala)n were synthesized by polymerization of active esters (1-succinimidyl or pentafluorophenyl) of the corresponding Nα-deblocked monomers. The monomers were prepared using the usual methods of peptide synthesis in solution. Upon dialysis, the average molecular weight of the polymer was 6 000-9 000 as determined by sedimentation in ultracentrifuge. Polypeptides, containing leucine in addition to the basic amino acid, showed a marked tendency to aggregation. CD spectra of the products were measured for characterization.

Use of 4-chlorobutyl esters in peptide synthesis

1990 ◽  
Vol 55 (9) ◽  
pp. 2357-2359 ◽  
Author(s):  
M. Joaquina S. A. Amaral Trigo ◽  
M. Isabel A. Oliveira Santos
Keyword(s):  
Peptide Synthesis

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