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Divergent strategy in marine tetracyclic meroterpenoids synthesis
ReviewAbstract: The divergent total synthesis strategy can be successfully applied to the preparation of families ofPalabras claves:Aureol, Divergent total synthesis, marine natural products, Tetracyclic meroterpenoidsAutores:Antonio Rosales Martínez, López-Martínez J.L., Rodríguez-García I.Fuentes:scopusTotal synthesis of (±)-euryfuran through Ti(III) catalyzed radical cyclization
ArticleAbstract: A concise total synthesis of the furano-sesquiterpene (±)-euryfuran, a bioactive metabolite from somPalabras claves:Cyclization, Diastereoselectivity, Farnesol, Furanosesquiterpenes, Radical reactions, titaniumAutores:Alvarez-Corral M., Antonio Rosales Martínez, López-Sánchez C., Muñoz-Dorado M., Rodríguez-García I.Fuentes:scopusUnifying the Synthesis of a Whole Family of Marine Meroterpenoids through a Biosynthetically Inspired Sequence of 1,2-Hydride and Methyl Shifts as Key Step
ArticleAbstract: Marine meroterpenoids have attracted a great deal of attention from synthetic research groups due toPalabras claves:marine natural products, meroterpenoids, rearrangements, synthetic strategiesAutores:Antonio Rosales Martínez, Rodríguez-García I., Roman Nicolay Rodríguez-MaeckerFuentes:scopus