Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations-Reference-Cited by-同舟云学术

Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations

Published:2021 Issue:7 Volume:57 Page:899-902
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yoshida Suguru¹²³⁴⁵^ORCID,Sakata Yuki¹²³⁴⁵,Misawa Yoshihiro¹²³⁴⁵,Morita Takamoto¹²³⁴⁵,Kuribara Tomoko¹²³⁴⁵,Ito Harumi¹²³⁴⁵,Koike Yuka⁶⁷⁸⁹⁵,Kii Isao¹⁰¹¹¹²¹³⁹,Hosoya Takamitsu¹²³⁴⁵^ORCID

Affiliation:

1. Laboratory of Chemical Bioscience

2. Institute of Biomaterials and Bioengineering

3. Tokyo Medical and Dental University (TMDU)

4. Chiyoda-ku

5. Japan

6. Common Facilities Unit

7. Compass to Healthy Life Research Complex Program

8. RIKEN Cluster for Science and Technology Hub

9. Chuo-ku

10. Pathophysiological and Health Science Team

11. Division of Bio-Function Dynamics Imaging

12. Imaging Platform and Innovation Group

13. RIKEN Center for Life Science Technologies (CLST)

Abstract

Efficient consecutive 1,2,3-triazole formations using multiazide platforms are disclosed. A convergent synthesis of tetrafunctionalized probes was achieved from a tetraazide platform in a modular synthetic manner.

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/2021/CC/D0CC07789E

Reference52 articles.

1. J. Lahann , Click Chemistry for Biotechnology and Materials Science , John Wiley & Sons , West Sussex , 2009

2. Molecular Scaffolds Using Multiple Orthogonal Conjugations: Applications in Chemical Biology and Drug Discovery

3. Inverse electron demand Diels–Alder (iEDDA)-initiated conjugation: a (high) potential click chemistry scheme

4. Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry

5. Controlled Reactive Intermediates Enabling Facile Molecular Conjugation

Cited by 13 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. Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction;European Journal of Organic Chemistry;2024-06-18

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

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

4. Five-membered ring systems: with more than one N atom;Progress in Heterocyclic Chemistry;2023

5. Development of Synthetic Chemistry on Organic Azides by Breaking their 1,3-Dipolar Characteristics;Journal of Synthetic Organic Chemistry, Japan;2022-12-01