Facile selective synthesis of 2-methyl-5-amino-1,2,4-oxadiazolium bromides as further targets for nucleophilic additions-Reference-Cited by-同舟云学术

Facile selective synthesis of 2-methyl-5-amino-1,2,4-oxadiazolium bromides as further targets for nucleophilic additions

Published:2018 Issue:12 Volume:42 Page:9373-9376
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Il’in Mikhail V.¹²³^ORCID,Bolotin Dmitrii S.¹²³^ORCID,Suslonov Vitalii V.⁴⁵²³^ORCID,Kukushkin Vadim Yu.¹²³^ORCID

Affiliation:

1. Institute of Chemistry, Saint Petersburg State University

2. Saint Petersburg

3. Russian Federation

4. Center for X-ray Diffraction Studies

5. Saint Petersburg State University

Abstract

The reaction of aminonitrones with isocyanides and Br₂ gives 2-methyl-5-amino-1,2,4-oxadiazolium bromides, which are convenient precursors for other heterocycles and ureides.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ01682H

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