Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/63873
Type: Artigo de Periódico
Title: Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones
Authors: Guilherme Augusto de Melo Jardim
Willian Xerxes Coelho Oliveira
Rossimiriam Pereira de Freitas
Rubem Figueiredo Sadok Menna Barreto
Thaissa Lúcio Silva
Marilia Oliveira Fonseca Goulart
Eufrânio Nunes da Silva Júnior
Abstract: We report a sequential C–H iodination/organoyl-thiolation of naphthoquinones and their relevant trypanocidal activity. Under a combination of AgSR with a copper source, sulfur-substituted benzenoid quinones were prepared in high yields (generally >90%). This provides an efficient and general method for preparing A-ring modified naphthoquinoidal systems, recognized as a challenge in quinone chemistry.
Subject: Química orgânica
Quinona
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: ICX - DEPARTAMENTO DE QUÍMICA
Rights: Acesso Restrito
metadata.dc.identifier.doi: https://doi.org/10.1039/C8OB00196K
URI: http://hdl.handle.net/1843/63873
Issue Date: 2018
metadata.dc.url.externa: https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00196k
metadata.dc.relation.ispartof: Organic & Biomolecular Chemistry
Appears in Collections:Artigo de Periódico

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