AN EFFICIENT SYNTHESIS OF 2,4'-BI-1,3-OXA(THIA)ZOLES AS SCAFFOLDS FOR BIOACTIVE PRODUCTS
DOI:
https://doi.org/10.1007/1508Ключевые слова:
bi-1, 3-azoles, α-halo ketone, β-hydroxy amides, Hantzsch reaction, oxidative cyclodehydrationАннотация
A rapid and efficient methodology to prepare 2,4'-bi-1,3-azoles as scaffolds for biologically active marine natural products is described. Hantzsch reaction and oxidative cyclodehydration of β-hydroxy amides or thioamides were used to construct the azole rings. The obtained biheterocycles displayed no cytotoxicity on HCT-15 cell line.
Also published in Chemistry of Heterocyclic Compounds, 2011, 47 (6), pp 703-709
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Опубликован
2014-01-21
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Оригинальные статьи