A one-pot route to N-acyl ureas: a formal four-component hydrolytic reaction involving aminonitrones and isocyanide dibromides-Reference-Cited by-同舟云学术

A one-pot route to N-acyl ureas: a formal four-component hydrolytic reaction involving aminonitrones and isocyanide dibromides

Published:2020 Issue:4 Volume:44 Page:1253-1262
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Il’in Mikhail V.¹²³⁴^ORCID,Lesnikova Liana A.¹²³⁴^ORCID,Bolotin Dmitrii S.¹²³⁴^ORCID,Novikov Alexander S.¹²³⁴^ORCID,Suslonov Vitalii V.⁵²³⁴^ORCID,Kukushkin Vadim Yu.¹²³⁴^ORCID

Affiliation:

1. Institute of Chemistry

2. Saint Petersburg State University

3. Saint Petersburg

4. Russian Federation

5. Center for X-ray Diffraction Studies

Abstract

A one-pot route to N-acyl ureas proceeds via generation of electrophilically activated 2-substituted 1,2,4-oxadiazolium salts. The conformation of the N-acyl ureas is stabilized via moderate strength (6.2–7.8 kcal mol⁻¹) resonance-assisted hydrogen bonds.

Funder

Russian Foundation for Basic Research

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/C9NJ05445F

Reference81 articles.

1. Gelling and the collective dynamics in ferroelectric liquid crystals

2. Controlled fabrication of organic nanotubes via self-assembly of non-symmetric bis-acylurea