4.8 Article

Pd(II)-Catalyzed Intramolecular Tandem Olefin Amidation/C-H Activation Protocol for the Syntheses of the Protoberberine Class of Natural Products

Journal

ORGANIC LETTERS
Volume 18, Issue 15, Pages 3862-3865

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01868

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Funding

  1. UGC-New Delhi
  2. DST, New Delhi
  3. CSIR-ORIGIN, New Delhi

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A Pd(II)-catalyzed intramolecular tandem olefin amidation/C-H activation protocol has been developed for the synthesis of an 8-oxoprotoberberine core. It was successfully applied for the syntheses of (+/-)-8-oxocanadine, (+/-)-8-oxotetrahydropalmitine, and (+/-)-8-oxostylopine, which can be easily converted to the respective protoberberine natural products. The short synthetic route demonstrated would be useful for the synthesis of a large number of natural products and their analogues featuring a protoberberine scaffold.

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