Decarboxylative ring-opening of 2-oxazolidinones: a facile and modular synthesis of β-chalcogen amines-Reference-Cited by-同舟云学术

Decarboxylative ring-opening of 2-oxazolidinones: a facile and modular synthesis of β-chalcogen amines

Published:2022 Issue:53 Volume:12 Page:34496-34502
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Galetto Fábio Z.¹^ORCID,da Silva Cleiton¹,Beche Ricardo I. M.¹,Balaguez Renata A.¹,Franco Marcelo S.¹^ORCID,de Assis Francisco F.¹,Frizon Tiago E. A.²,Su Xiao³^ORCID

Affiliation:

1. Department of Chemistry, Federal University of Santa Catarina, Florianópolis, SC, 88040-900, Brazil

2. Department of Energy and Sustainability, Federal University of Santa Catarina, Araranguá, SC, Brazil

3. Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA

Abstract

This study includes a new protocol for the synthesis of primary and secondary β-chalcogen amines (Se, Te and S) from the ring-opening reaction of non-activated 2-oxazolidinones with chalcogenolate anions.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Division of Chemical, Bioengineering, Environmental, and Transport Systems

Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA06070A

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