Detalhes do Documento

A new strategy for the synthesis of 3-cinnamoyl-2-styrylchromones and their tra...

Autor(es): Pinto, Diana C. G. A. cv logo 1 ; Seca, Ana M. L. cv logo 2 ; Leal, Stephanie B. cv logo 3 ; Silva, Artur M. S. cv logo 4 ; Cavaleiro, José A. S. cv logo 5

Data: 2011

Identificador Persistente: http://hdl.handle.net/10400.3/2922

Origem: Repositório da Universidade dos Açores

Assunto(s): Xanthenodiones; Synthesis


Descrição
23rd ISHC Congress will be held in Glasgow, Scotland from July 31 August 4, 2011. Chromones are a class of oxygen heterocyclic compounds widely distributed in Nature. 2-Styrylchromones are, however, a small and rare naturally occurring chromones; only three derivatives have been isolated, two from the marine blue green algae Chrysophaeum taylori1 and one from the rhizomes of Imperata cylindrical. Even so, 2-styrylchromone derivatives are associated with noticeable biological activities. Our group has also been interested in the synthesis and biological evaluation of 3-aroylflavones and found that 3’,4’,5,7-tetrahydroxy-3-(3,4-dihydroxybenzoyl)flavone is a potential antioxidant agent. As part of our continuing work on the synthesis and antioxidant evaluations of polyhydroxy-2-styrylchromones,4 we set up a program aiming the synthesis of 3-cinnamoyl-2-styrylchromone (2) bearing hydroxyl groups, features considered essential to be good antioxidant and anti-inflammatory agents.
Tipo de Documento Documento de conferência
Idioma Inglês
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