4.8 Article

Total Syntheses of Festuclavine, Pyroclavine, Costaclavine, epi-Costaclavine, Pibocin A, 9-Deacetoxyfumigaclavine C, Fumigaclavine G, and Dihydrosetoclavine

Journal

ORGANIC LETTERS
Volume 19, Issue 12, Pages 3323-3326

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01504

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Funding

  1. National Natural Science Foundation of China [21372017, 21402003, 21290183, 21572008]
  2. State Key Laboratory of Drug Research

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A new approach for the divergent total synthesis of eight ergot alkaloids is reported. The approach allows the first total syntheses of pyroclavine, pibocin A, 9-deacetoxyfumigaclavine C, and fumigaclavine G and also enables the efficient synthesis of festuclavine, costaclavine, epi-costaclavine, and dihydrosetoclavine. The main feature of the synthesis is the use of an unprecedented Pd-catalyzed intramolecular Larock indole annulation/TsujiTrost allylation cascade to assemble the tetracyclic core in one step.

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