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Dyotropic rearrangements in natural product total synthesis and biosynthesis

Journal

NATURAL PRODUCT REPORTS
Volume 34, Issue 3, Pages 228-234

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7np00005g

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Funding

  1. Funds of the Chemical Industry (Sachkostenzuschuss and Dozentenpreis)
  2. German Research Foundation (Emmy Noether Fellowship) [SFB 749, SFB 152]

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This highlight article presents some recent examples of dyotropic rearrangements, which were applied in natural product total synthesis or proposed to occur in biosyntheses. The implementation of dyotropic reactions in the preparation of complex natural products has resulted in the development of elegant synthetic routes, and thereby highlights the utility of these powerful, yet relatively underrepresented, transformations.

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