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Enantioselective Total Synthesis of Nigelladine A via Late-Stage C–H Oxidation Enabled by an Engineered P450 Enzyme

An enantioselective total synthesis of the norditerpenoid alkaloid nigelladine A is described. Strategically, the synthesis relies on a late stage C-H oxidation of an advanced intermediate. While traditional chemical methods failed to deliver the desired outcome, an engineered cytochrome P450 enzyme...

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Detalhes bibliográficos
Publicado no:J Am Chem Soc
Main Authors: Loskot, Steven A., Romney, David K., Arnold, Frances H., Stoltz, Brian M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5679227/
https://ncbi.nlm.nih.gov/pubmed/28721734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.7b05196
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