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Total synthesis and stereochemical revision of acortatarins A and B
Authors:Sudhakar Gangarajula  Kadam Vilas D  Bayya Shruthi  Pranitha Gavinolla  Jagadeesh Bharatam
Institution:Organic Chemistry Division-II, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 607, India. gsudhakar@iict.res.in
Abstract:A first total synthesis of acortatarins A, B, and an enantiomer of the proposed structure of acortatarin B is described by using readily available d-sugars. This convergent total synthesis revealed the revision of the absolute configuration of acortatarin A and structural revision of acortatarin B. The key steps involved are regioselective epoxide opening with deprotonated 2,5-disubstituted pyrrole and spiroketalization.
Keywords:
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