Regioselective construction of pyridazine and tetrahydrocinnoline derivatives via [4 + 2] cycloaddition–elimination with α-halogeno hydrazones and enaminones-Reference-Cited by-同舟云学术

Regioselective construction of pyridazine and tetrahydrocinnoline derivatives via [4 + 2] cycloaddition–elimination with α-halogeno hydrazones and enaminones

Published:2020 Issue:16 Volume:7 Page:2307-2312
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Duan Liancheng¹²³⁴,Wang Xin¹²³⁴,Gu Yucheng⁵⁶⁷,Hou Yunlei¹²³⁴,Gong Ping¹²³⁴^ORCID

Affiliation:

1. School of Pharmaceutical Engineering

2. Shenyang Pharmaceutical University

3. Shenyang

4. China

5. Syngenta Jealott's Hill International Research Center

6. Berkshire RG42 6EY

7. UK

Abstract

Herein, we report the de novo construction of pyridazine scaffolds via a [4 + 2] cycloaddition–elimination reaction with α-halogeno hydrazones and enaminones.

Funder

Ministry of Education of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00555J

Reference51 articles.

1. Aminopyridazines as Acetylcholinesterase Inhibitors

2. Polytopic ligand directed self-assembly—polymetallic [n×n] grids versus non-grid oligomers

3. Self-Assembly of a Cu4 Complex with Coplanar Copper(I) Ions: Synthesis, Structure, and Electrochemical Properties