Facilitating Myers–Saito cyclization through acid-triggered tautomerization for the development of maleimide-based antitumor agents
Author:
Affiliation:
1. Shanghai Key Laboratory of Advanced Polymeric Materials
2. School of Materials Science and Engineering
3. East China University of Science and Technology
4. Shanghai 200237
5. China
Abstract
Enyne-allene compounds undergo Myers–Saito cyclization at physiological temperature to generate diradical intermediates that are capable of inducing DNA damage and cell death.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Shanghai Leading Academic Discipline Project
Publisher
Royal Society of Chemistry (RSC)
Subject
General Materials Science,Biomedical Engineering,General Chemistry,General Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/2020/TB/C9TB02589H
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