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Total Synthesis of Dixiamycin B by Electrochemical Oxidation

[Image: see text] N–N-linked dimeric indole alkaloids represent an unexplored class of natural products for which chemical synthesis has no practical solution. To meet this challenge, an electrochemical oxidative dimerization method was developed, which was applied as the pivotal step of the first t...

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Detalles Bibliográficos
Autores principales: Rosen, Brandon R., Werner, Erik W., O’Brien, Alexander G., Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004216/
https://www.ncbi.nlm.nih.gov/pubmed/24697810
http://dx.doi.org/10.1021/ja5013323
Descripción
Sumario:[Image: see text] N–N-linked dimeric indole alkaloids represent an unexplored class of natural products for which chemical synthesis has no practical solution. To meet this challenge, an electrochemical oxidative dimerization method was developed, which was applied as the pivotal step of the first total synthesis of dixiamycin B. This method is also general for N–N dimerization of substituted carbazoles and β-carbolines, providing entry into seldom explored chemical space.