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An expedient enantioselective strategy for the oxatetracyclic core of platensimycin
Authors:Kaliappan Krishna P  Ravikumar Velayutham
Affiliation:Department of Chemistry, Indian Institute of Technology-Bombay, Powai, Mumbai, India. kpk@chem.iitb.ac.in
Abstract:An enantioselective route for the synthesis of oxatetracyclic core of platensimycin is reported for the first time using a 5-exo-trig cyclization followed by intramolecular etherification as key reactions. The requisite dienynone for the radical cyclization is synthesized in eight steps from the Wieland-Miescher ketone employing a Claisen rearrangement.
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