Peptide coupling using recyclable bicyclic benziodazolone-Reference-Cited by-同舟云学术

Peptide coupling using recyclable bicyclic benziodazolone

Published:2024 Issue:8 Volume:60 Page:956-959
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Uehara Daigo¹,Adachi Sota²,Tsubouchi Akira¹,Okada Yohei²^ORCID,Zhdankin Viktor V.³^ORCID,Yoshimura Akira⁴^ORCID,Saito Akio¹^ORCID

Affiliation:

1. Division of Applied Chemistry, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan

2. Department of Applied Biological Science, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8509, Japan

3. Department of Chemistry and Biochemistry, University of Minnesota, Duluth, MN, 55812, USA

4. Faculty of Pharmaceutical Sciences, Aomori University, 2-3-1 Kobata, Aomori 030-0943, Japan

Abstract

This study provides a greener peptide coupling method using triarylphosphine and recyclable bicyclic benziodazolone, which acts as an oxidant for phosphine as well as base.

Funder

Core Research for Evolutional Science and Technology

Iketani Science and Technology Foundation

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D3CC04431A

Reference41 articles.

1. Nonclassical Routes for Amide Bond Formation

2. Sustainable Amidation Reactions - Recent Advances

3. Sustainability Challenges in Peptide Synthesis and Purification: From R&D to Production

4. Liquid-Phase Peptide Synthesis (LPPS): A Third Wave for the Preparation of Peptides

5. Peptide Coupling Reagents, More than a Letter Soup

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