RESUMEN
The chemical modification of structurally complex fermentation products, a process known as semisynthesis, has been an important tool in the discovery and manufacture of antibiotics for the treatment of various infectious diseases. However, many of the therapeutics obtained in this way are no longer effective, because bacterial resistance to these compounds has developed. Here we present a practical, fully synthetic route to macrolide antibiotics by the convergent assembly of simple chemical building blocks, enabling the synthesis of diverse structures not accessible by traditional semisynthetic approaches. More than 300 new macrolide antibiotic candidates, as well as the clinical candidate solithromycin, have been synthesized using our convergent approach. Evaluation of these compounds against a panel of pathogenic bacteria revealed that the majority of these structures had antibiotic activity, some efficacious against strains resistant to macrolides in current use. The chemistry we describe here provides a platform for the discovery of new macrolide antibiotics and may also serve as the basis for their manufacture.
Asunto(s)
Antibacterianos/síntesis química , Antibacterianos/farmacología , Descubrimiento de Drogas/métodos , Macrólidos/síntesis química , Macrólidos/farmacología , Amino Azúcares/síntesis química , Amino Azúcares/química , Amino Azúcares/farmacología , Antibacterianos/química , Bacterias/efectos de los fármacos , Humanos , Cetólidos/síntesis química , Cetólidos/química , Macrólidos/química , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Bibliotecas de Moléculas Pequeñas/síntesis química , Bibliotecas de Moléculas Pequeñas/química , Triazoles/síntesis química , Triazoles/química , Triazoles/farmacologíaRESUMEN
The first synthesis of (±)-tetrapetaloneâ A-Me aglycon is described. Key bond-forming reactions include Nazarov cyclization, a ring-closing metathesis promoted with complete diastereoselectivity by a chiral molybdenum-based complex, tandem conjugate reduction/intramolecular aldol cyclization, and oxidative dearomatization.
Asunto(s)
Glicósidos/síntesis química , Compuestos Heterocíclicos de 4 o más Anillos/síntesis química , Ciclización , Glicósidos/química , Compuestos Heterocíclicos de 4 o más Anillos/química , Conformación Molecular , Molibdeno/química , Compuestos Organometálicos/química , EstereoisomerismoRESUMEN
A heterogeneous gold catalyst with remarkable activity for promoting the electrophilic reactions of aryl vinyl ketones and aryl dienyl ketones is described. The catalyst is easy to prepare, is robust, and can be recycled. Low loadings are effective for different types of cationic reactions, including Nazarov cyclizations, lactonizations, and [1,2] shifts.