Tandem C–H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (−)-brussonol and (−)-przewalskine E

Natural products are a vital source of lead compounds in drug discovery. Development of efficient tandem reactions to build useful compounds and apply them to the synthesis of natural products is not only a significant challenge but also an important goal for chemists. Here we describe a tandem C–H...

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Detalles Bibliográficos
Autores principales: Jiao, Zhi-Wei, Tu, Yong-Qiang, Zhang, Qing, Liu, Wen-Xing, Zhang, Shu-Yu, Wang, Shao-Hua, Zhang, Fu-Min, Jiang, Sen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557391/
https://www.ncbi.nlm.nih.gov/pubmed/26081438
http://dx.doi.org/10.1038/ncomms8332

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557391/
https://www.ncbi.nlm.nih.gov/pubmed/26081438
http://dx.doi.org/10.1038/ncomms8332

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