ChemInform Abstract: CROWN ETHERS AS CATALYSTS OF FLUORIDE-ANION-MEDIATED REACTIONS IN PEPTIDE SYNTHESIS. PART 1. PROTECTION OF TRYPTOPHAN BY BENZYLOXYCARBONYL AND 2,4-DICHLOROBENZYLOXYCARBONYL GROUPS

1977 ◽  
Vol 8 (25) ◽  
pp. no-no
Author(s):  
Y. S. KLAUSNER ◽  
M. CHOREV
Keyword(s):  
Peptide Synthesis ◽  
Crown Ethers ◽  
Fluoride Anion

Crown ethers and peptide synthesis

Peptides 1994 ◽  
1995 ◽  
pp. 147-148
Author(s):  
P. Botti ◽  
H. L. Ball ◽  
P. Lucietto ◽  
M. Pinori ◽  
P. Mascagni
Keyword(s):  
Peptide Synthesis ◽  
Crown Ethers

CHEMICAL EFFECTS IN MULTIELECTRON PROCESSES IN THE FLUORIDE ANION

1987 ◽  
Vol 48 (C9) ◽  
pp. C9-777-C9-780
Author(s):  
R. HESSABI ◽  
D. URCH
Keyword(s):  
Fluoride Anion ◽  
Chemical Effects

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>

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