Synthesis of 2-Aminofurans by Sequential [2+2] Cycloaddition-Nucleophilic Addition of 2-Propyn-1-ols with Tetracyanoethylene and Amine-Induced Transformation into 6-Aminopentafulvenes-Reference-Cited by-同舟云学术

Synthesis of 2-Aminofurans by Sequential [2+2] Cycloaddition-Nucleophilic Addition of 2-Propyn-1-ols with Tetracyanoethylene and Amine-Induced Transformation into 6-Aminopentafulvenes

Published:2017-03-23 Issue:21 Volume:23 Page:5126-5136
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Shoji Taku¹^ORCID,Nagai Daichi¹,Tanaka Miwa¹,Araki Takanori¹,Ohta Akira¹,Sekiguchi Ryuta²,Ito Shunji²,Mori Shigeki³,Okujima Tetsuo⁴^ORCID

Affiliation:

1. Department of Material Science; Graduate School of Science and Technology; Shinshu University, Matsumoto; 390-8621 Nagano Japan

2. Graduate School of Science and Technology; Hirosaki University, Hirosaki; 036-8561 Aomori Japan

3. Advanced Research Support Center; Ehime University, Matsuyama; 790-8577 Ehime Japan

4. Department of Chemistry and Biology; Graduate School of Science and Engineering; Ehime University, Matsuyama; 790-8577 Ehime Japan

Funder

Japan Society for the Promotion of Science (JSPS)

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference110 articles.

1. Discovery of 7-Methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (GSK2606414), a Potent and Selective First-in-Class Inhibitor of Protein Kinase R (PKR)-like Endoplasmic Reticulum Kinase (PERK)

2. Discovery of Small Molecule RIP1 Kinase Inhibitors for the Treatment of Pathologies Associated with Necroptosis

3. Optimization of Ligand and Lipophilic Efficiency To Identify an in Vivo Active Furano-Pyrimidine Aurora Kinase Inhibitor

4. Heterocyclen aus CH‐aciden Nitrilen, IX. Über die Reaktion von α‐Hydroxy‐ketonen mit Malodinitril

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