Facile preparation of 3,5-disubstituted-4-aminothiophene-2-carbaldehyde from a novel unexpected domino reaction of vinyl azides and 1,4-dithiane-2,5-diol-Reference-Cited by-同舟云学术

Facile preparation of 3,5-disubstituted-4-aminothiophene-2-carbaldehyde from a novel unexpected domino reaction of vinyl azides and 1,4-dithiane-2,5-diol

Published:2014 Issue:84 Volume:4 Page:44462-44465
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Chen Binhui¹²³⁴,Ni Hangcheng¹²³⁴,Guo Xiao¹²³⁴,Zhang Guolin¹²³⁴,Yu Yongping¹²³⁴

Affiliation:

1. Zhejiang Province Key Laboratory of Anti-Cancer Drug Research

2. College of Pharmaceutical Science

3. Zhejiang University

4. Hangzhou 310058, P. R. China

Abstract

A facile approach to provide 3,5-disubstituted-4-aminothiophene-2-carbaldehyde containing both the amino group and the aldehyde group has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA08649J

Reference45 articles.

1. 2-Amino-3-benzoylthiophene Allosteric Enhancers of A1 Adenosine Agonist Binding: New 3, 4-, and 5-Modifications

2. Hybrid Ortho/Allosteric Ligands for the Adenosine A1 Receptor

3. Identification of Novel Falcipain-2 Inhibitors as Potential Antimalarial Agents through Structure-Based Virtual Screening

4. 2-aminothiophenes by the gewald reaction

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