Introduction of alkyl substituents to aromatic compounds
US-10351492-B2 · Jul 16, 2019 · US
US9023957B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9023957-B2 |
| Application number | US-201113808303-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 6, 2011 |
| Priority date | Jul 6, 2010 |
| Publication date | May 5, 2015 |
| Grant date | May 5, 2015 |
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The present invention generally relates to processes and methods of peptide and protein synthesis. The present invention also relates to specific compounds for use in such processes and methods. It is shown herein that peptides with a C-terminal tertiary N,N-bis(2-mercaptoethyl)-amide (BMEA) undergo N-to-S acyl transfer at weakly acidic pH to form a transient thioester which can be captured for direct ligation with a cysteinyl peptide. These C-terminal BMEA peptides are easily prepared with standard Fmoc solid-phase synthesis protocols, thus giving a very convenient access to the thioester components for native chemical ligation.
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The invention claimed is: 1. A method of peptide synthesis comprising a step of reacting a compound to form a polypeptide or protein, the compound having the following structural formula: wherein n is 2 or 3; m is 2 or 3; and RC(O)— is an amino acyl or peptidyl group, or R is selected from the group consisting of hydrogen, oxygen, sulfur, alkyl, al…
Chemistry & Metallurgy · mapped topic
Chemistry & Metallurgy · mapped topic
Chemistry & Metallurgy · mapped topic
Chemistry & Metallurgy · mapped topic
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