Sequential conjugation methods based on triazole formation and related reactions using azides-Reference-Cited by-同舟云学术

Sequential conjugation methods based on triazole formation and related reactions using azides

Published:2020 Issue:8 Volume:18 Page:1550-1562
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yoshida Suguru¹²³⁴⁵^ORCID

Affiliation:

1. Laboratory of Chemical Bioscience

2. Institute of Biomaterials and Bioengineering

3. Tokyo Medical and Dental University (TMDU)

4. Tokyo 101-0062

5. Japan

Abstract

This review highlights recent transformations involving selective triazole formation, allowing efficient preparation of unsymmetric bis- and tris(triazole)s using diverse platform molecules.

Funder

Japan Society for the Promotion of Science

Naito Foundation

Japan Agency for Medical Research and Development

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/C9OB02698C

Reference126 articles.

1. The Staudinger Ligation—A Gift to Chemical Biology

2. Thiol-Ene Click Chemistry

3. Staudinger Ligation as a Method for Bioconjugation

4. Bioconjugation via azide–Staudinger ligation: an overview

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Amphos-Mediated Conversion of Alkyl Azides to Diazo Compounds and One-Pot Azide-Site Selective Transient Protection, Click Conjugation, and Deprotective Transformation;Organic Letters;2024-03-19

2. N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition;Angewandte Chemie;2024-02-12

3. N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition;Angewandte Chemie International Edition;2024-02-12

4. Iterative click reactions using trivalent platforms for sequential molecular assembly;Chemical Communications;2024

5. Click assembly through selective azaylide formation;Chemical Communications;2024