A versatile catalyst-free perfluoroaryl azide–aldehyde–amine conjugation reaction-Reference-Cited by-同舟云学术

A versatile catalyst-free perfluoroaryl azide–aldehyde–amine conjugation reaction

Published:2019 Issue:2 Volume:3 Page:251-256
ISSN:2052-1537
Container-title:Materials Chemistry Frontiers
language:en
Short-container-title:Mater. Chem. Front.

Author:

Xie Sheng¹²³⁴⁵^ORCID,Zhou Juan¹²³⁴⁶^ORCID,Chen Xuan¹⁷⁸⁹,Kong Na¹²³⁴^ORCID,Fan Yanmiao¹²³⁴,Zhang Yang¹²³⁴,Hammer Gerry¹⁰¹¹¹²¹³¹⁴,Castner David G.¹⁰¹¹¹²¹³¹⁴,Ramström Olof¹²³⁴¹^ORCID,Yan Mingdi¹²³⁴¹^ORCID

Affiliation:

1. Department of Chemistry

2. KTH-Royal Institute of Technology

3. Stockholm

4. Sweden

5. College of Chemistry and Chemical Engineering

6. Key Laboratory of Carbohydrate Chemistry and Biotechnology

7. University of Massachusetts Lowell

8. Lowell

9. USA

10. National ESCA and Surface Analysis Center for Biomedical Problems

11. Departments of Bioengineering and Chemical Engineering

12. University of Washington

13. Seattle

14. Washington

Abstract

In a tri-component reaction, an electrophilically-activated perfluoroaryl azide, an aldehyde and an amine react readily to yield a stable amidine conjugate.

Funder

Kungliga Tekniska Högskolan

National Institutes of Health

National Science Foundation

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Materials Science

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QM/C8QM00516H

Reference80 articles.