Phototriggered base proliferation: a powerful 365 nm LED photoclick tool for nucleophile-initiated thiol-Michael addition reaction-Reference-Cited by-同舟云学术

Phototriggered base proliferation: a powerful 365 nm LED photoclick tool for nucleophile-initiated thiol-Michael addition reaction

Published:2017 Issue:2 Volume:7 Page:914-918
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Xu Ruixin¹²³⁴,Guan Xiaoyuan⁵⁶⁷⁴,He Minghui⁵⁶⁷⁴,Yang Jianwen⁸⁹⁷⁴

Affiliation:

1. School of Media and Communication

2. Shenzhen Polytechnic

3. Shenzhen

4. China

5. State Key Laboratory of Pulp & Paper Engineering

6. South China University of Technology

7. Guangzhou

8. DSAPM Lab, School of Materials Science and Engineering

9. Sun Yat-Sen University

Abstract

The phototriggered base proliferation (PBP) reaction as a powerful 365 nm LED photoclick tool is presented for nucleophile-initiated thiol-Michael addition reaction.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C6RA25906E

Reference25 articles.

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

2. The growing applications of click chemistry

3. Thiol-Ene Click Chemistry

4. Nucleophile-Initiated Thiol-Michael Reactions: Effect of Organocatalyst, Thiol, and Ene

5. Investigation into thiol-(meth)acrylate Michael addition reactions using amine and phosphine catalysts

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