Catalyst-free inverse-electron-demand aza-Diels–Alder reaction of 4,4-dicyano-2-methylenebut-3-enoates and 1,3,5-triazinanes: access to polysubstituted tetrahydropyridines-Reference-Cited by-同舟云学术

Catalyst-free inverse-electron-demand aza-Diels–Alder reaction of 4,4-dicyano-2-methylenebut-3-enoates and 1,3,5-triazinanes: access to polysubstituted tetrahydropyridines

Published:2023 Issue:26 Volume:21 Page:5413-5418
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yang Dezhi¹²^ORCID,Zhu Meng¹²,Wang Taimin²,He Yixuan²,Xie Lang¹²,Zhang Jiayong²,Cheng Bin¹²^ORCID

Affiliation:

1. School of Pharmacy, Zunyi Medical University, Zunyi 563000, China

2. Institute of Marine Biomedicine/Postdoctoral Innovation Practice Base, Shenzhen Polytechnic, Shenzhen 518055, China

Abstract

An inverse-electron-demand aza-Diels–Alder reaction between 4,4-dicyano-2-methylenebut-3-enoates and 1,3,5-triazinanes under catalyst-free and additive-free conditions was developed.

Funder

Department of Education of Guangdong Province

Science, Technology and Innovation Commission of Shenzhen Municipality

Shenzhen Polytechnic

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00511A

Reference88 articles.

1. The discovery of tetrahydropyridine analogs as h Nav1.7 selective inhibitors for analgesia