4.8 Article

FeCl3 Catalyzed Prins-Type Cyclization for the Synthesis of Highly Substituted Indenes: Application to the Total Synthesis of (±)-Jungianol and epi-Jungianol

Journal

ORGANIC LETTERS
Volume 15, Issue 3, Pages 429-431

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol3032347

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Funding

  1. CSIR, New Delhi
  2. IIT Kanpur

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A novel approach was developed for the synthesis of highly substituted indene derivatives, using an FeCl3 catalyzed Prins-type cyclization reaction which was further applied in the total synthesis of jungianol and epi-jungianol.

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