Development of a safely handleable synthetic equivalent of cyanonitrile oxide by 1,3-dipolar cycloaddition of nitroacetonitrile-Reference-Cited by-同舟云学术

Development of a safely handleable synthetic equivalent of cyanonitrile oxide by 1,3-dipolar cycloaddition of nitroacetonitrile

Published:2019 Issue:55 Volume:55 Page:7903-7905
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Nishiwaki Nagatoshi¹²³⁴⁵^ORCID,Kumegawa Yuta¹²³,Iwai Kento¹²³^ORCID,Yokoyama Soichi¹²³⁴⁵^ORCID

Affiliation:

1. School of Environmental Science and Engineering, Kochi University of Technology

2. Kochi 782-8502

3. Japan

4. Research Center for Material Science and Engineering

5. Kochi University of Technology

Abstract

Cyano-aci-nitroacetate serves as a safely handleable precursor of nitroacetonitrile that undergoes 1,3-dipolar cycloaddition to form 3-cyanoisoxazol(in)es.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC03875B

Reference32 articles.

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3. Synthesis of 3-substituted 2-isoxazolines and 5,6-dihydro-4H-1,2-oxazines

4. Substituted 1-(isoxazol-3-yl)methyl-1H-1,2,3-triazoles: Synthesis, palladium(II) complexes, and high-turnover catalysis in aqueous media

5. Structure-Based Drug Design of Mineralocorticoid Receptor Antagonists to Explore Oxosteroid Receptor Selectivity

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