Azido-type-selective triazole formation by iridium-catalyzed cycloaddition with thioalkynes-Reference-Cited by-同舟云学术

Azido-type-selective triazole formation by iridium-catalyzed cycloaddition with thioalkynes

Published:2022 Issue:42 Volume:58 Page:6235-6238
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Sugiyama Kazuya¹,Sakata Yuki¹,Niwa Takashi¹²^ORCID,Yoshida Suguru¹^ORCID,Hosoya Takamitsu¹²^ORCID

Affiliation:

1. Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan

2. Laboratory for Chemical Biology, RIKEN Center for Biosystems Dynamics Research, 6-7-3 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan

Abstract

Iridium-catalyzed azide–thioalkyne cycloaddition was found to be effective for the azido-type-selective reaction of various multiazido compounds, enabling facile synthesis of multitriazole compounds in short steps.

Funder

Japan Agency for Medical Research and Development

Naito Foundation

Japan Society for the Promotion of Science

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/2022/CC/D2CC01739C

Reference36 articles.

1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

2. Click Chemistry in Complex Mixtures: Bioorthogonal Bioconjugation

3. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

4. Cu-Catalyzed Azide−Alkyne Cycloaddition

5. The CuAAC: Principles, Homogeneous and Heterogeneous Catalysts, and Novel Developments and Applications

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