Selective Peptide Chain Extension at the C-terminus of Aspartic and Glutamic Acids Utilizing N-protected (α-aminoacyl)benzotriazoles-Reference-Cited by-同舟云学术

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Selective Peptide Chain Extension at the C-terminus of Aspartic and Glutamic Acids Utilizing N-protected (α-aminoacyl)benzotriazoles

Published:2006-07 Issue:1 Volume:68 Page:42-47
ISSN:1747-0277
Container-title:Chemical Biology Drug Design
language:en
Short-container-title:Chem Biol Drug Design

Author:

Katritzky Alan R.,Todadze Ekaterina,Shestopalov Alexander A.,Cusido Janet,Angrish Parul

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Reference45 articles.

1. Biologically active peptides and enzymatic approaches to their production

2. Taste of free amino acids and peptides

3. Aspartame—a new food ingredient reply to the critical comments of woodrow C. Monte

4. Intense sweeteners for the food industry: an overview

5. Molecular design of inverted-aspartame-type sweeteners

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1. Synthetic access to thiolane-based therapeutics and biological activity studies;European Journal of Medicinal Chemistry;2021-11

2. Total synthesis and antimicrobial evaluation of natural albomycins against clinical pathogens;Nature Communications;2018-09-04

3. Acylbenzotriazoles: New Allies for Short Linear and Cyclic Peptide Constructs;Topics in Heterocyclic Chemistry;2016

4. Peptide Coupling Reagents, More than a Letter Soup;Chemical Reviews;2011-08-26

5. Chiral Acylation with N-(Protected α-Aminoacyl)benzotriazoles for Advantageous Syntheses of Peptides and Peptide Conjugates;Synlett;2009-08-28

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