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Rapid Access to the Tricyclic Core of Calyciphylline A‐Type Alkaloids Through Allyl Cyanate‐to‐Isocyanate Rearrangement
Journal article   Peer reviewed

Rapid Access to the Tricyclic Core of Calyciphylline A‐Type Alkaloids Through Allyl Cyanate‐to‐Isocyanate Rearrangement

D Baidilov, S Miskey and T Hudlicky
European Journal of Organic Chemistry, Vol.2019(46), pp.7590-7595
11/28/2019

Abstract

Concise and efficient synthetic route to the core of calyciphylline A‐type alkaloids is described herein. The aza‐[5,6,6] tricyclic framework of the Daphniphyllum subclass of these alkaloids was constructed featuring [1,3]‐Ichikawa transposition and intramolecular Heck cyclization protocols.
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Rapid Access to the Tricyclic Core of Calyciphylline A‐Type Alkaloids Through Allyl Cyanate‐to‐Isocyanate RearrangementView

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