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Efficient syntheses of streptocarpone and (±)-a-dunnione
(2007)
An efficient divergent synthesis of both streptocarpone and racemic α-dunnione from lawsone are described. A one-pot, formal [3+2] cyclization to form a furanonaphthoquinone directly provided a common intermediate.
Efficient syntheses of streptocarpone and (±)-a-dunnione
(2007)
An efficient divergent synthesis of both streptocarpone and racemic α-dunnione from lawsone are described. A one-pot, formal [3+2] cyclization to form a furanonaphthoquinone directly provided a common intermediate.
Synthesis and Antitumor Evaluation of Thiophene Analogs of Kigelinone
(BENTHAM SCIENCE PUBL LTD, 2009)
The synthesis of kigelinone thiophene analogs and related naphtho[2,3-b] thiophene-4,9-quinones from 2-substituted 4,7-dimethoxybenzo[b]thiophenes via an oxidative deprotection, Diels-Alder, and oxidative aromatization ...
Síntese de derivados de naftoquinonas com potencial atividade biologica.
(Universidade Federal de Minas GeraisBrasilFARMACIA - FACULDADE DE FARMACIAPrograma de Pós-Graduação em Ciências FarmacêuticasUFMG, 2022-03-28)
The naphthoquinones are substances widely distributed in nature and are endowed with
diverse biological activities, such as antifungal, antibacterial, anti-inflammatory,
antiplasmodial, trypanocidal and antitumor. Lapachol ...
Síntese e avaliação da atividade antitumoral de heterocíclicos furânicos, triazólicos e quinolínicos contendo o núcleo naftoquinona
(Universidade Federal de PernambucoUFPEBrasilPrograma de Pos Graduacao em Quimica, 2017)