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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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Detalhes bibliográficos
Publicado no:Nat Commun
Main Authors: Jiao, Zhi-Wei, Tu, Yong-Qiang, Zhang, Qing, Liu, Wen-Xing, Zhang, Shu-Yu, Wang, Shao-Hua, Zhang, Fu-Min, Jiang, Sen
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Pub. Group 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4557391/
https://ncbi.nlm.nih.gov/pubmed/26081438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms8332
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