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Six-membered ring systems: with O and/or S atoms

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Detalhes bibliográficos
Resumo:This chapter is dedicated to the synthesis of O- and S-6-membered heterocycles, covering the literature published during 2019. Highlights include the most interesting chemistry dedicated of these heterocyclic ring systems, from our personal point of view, with special emphasis to the synthesis of natural oxygen derivatives. Reviews on the isolation, biological properties, biosynthesis, and total synthesis of benzannulated spiroketal natural products (19OBC8272) and of diterpene pyran- 2-ones (19OBC8943), on the natural occurrence, pharmacological properties, and structureeactivity relationships of quassinoids, a kind of triterpenoid bearing a tetrahydropyran bridge (19CPB654), on the biosynthesis of Monascus azaphilone pigment congeners containing chromene frameworks (19NPR561), and on naturally occurring 3-aryl-4H-chromen-4-ones isolated after 2012 (19NPR1156), have appeared.
Autores principais:Santos, Clementina M.M.
Outros Autores:Silva, Artur
Assunto:Thio)pyrans Benzopyrans Chromones Coumarins Dioxanes
Ano:2021
País:Portugal
Tipo de documento:capítulo de livro
Tipo de acesso:acesso aberto
Instituição associada:Instituto Politécnico de Bragança
Idioma:inglês
Origem:Biblioteca Digital do IPB
Descrição
Resumo:This chapter is dedicated to the synthesis of O- and S-6-membered heterocycles, covering the literature published during 2019. Highlights include the most interesting chemistry dedicated of these heterocyclic ring systems, from our personal point of view, with special emphasis to the synthesis of natural oxygen derivatives. Reviews on the isolation, biological properties, biosynthesis, and total synthesis of benzannulated spiroketal natural products (19OBC8272) and of diterpene pyran- 2-ones (19OBC8943), on the natural occurrence, pharmacological properties, and structureeactivity relationships of quassinoids, a kind of triterpenoid bearing a tetrahydropyran bridge (19CPB654), on the biosynthesis of Monascus azaphilone pigment congeners containing chromene frameworks (19NPR561), and on naturally occurring 3-aryl-4H-chromen-4-ones isolated after 2012 (19NPR1156), have appeared.