Divergent Synthesis of Quinolone Natural Products from Pseudonocardia sp. CL38489

Two divergent synthetic routes are reported offering access to four quinolone natural products from Pseudonocardia sp. CL38489. Key steps to the natural products involved a regioselective epoxidation, an intramolecular Buchwald–Hartwig amination and a final acid‐catalysed 1,3‐allylic‐alcohol rearran...

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Detalles Bibliográficos
Autores principales: Geddis, Stephen M., Carro, Laura, Hodgkinson, James T., Spring, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215369/
https://www.ncbi.nlm.nih.gov/pubmed/28111524
http://dx.doi.org/10.1002/ejoc.201601195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215369/
https://www.ncbi.nlm.nih.gov/pubmed/28111524
http://dx.doi.org/10.1002/ejoc.201601195

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