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Total Synthesis of Dixiamycin B by Electrochemical Oxidation
Open accessAbstract
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.
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Metadata
- Authors
- Rosen, B. R., Werner, E. W., O’Brien, A. G., & Baran, P. S.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2014-04-08
- Volume
- 136
- Issue
- 15
- Pages
- 5571-5574
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2325214876
- Cited by
- 378
- References
- 0
- FWCI
- 10.46
- Type
- journal article
- Language
- en
- Open access
- hybrid
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