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Ti(III)-induced radical cyclization. A stereoselective entry to the perhydrobenzo[e]indene unit of new protein farnesyltransferase inhibitors, andrastins A-D
Authors:Masahiro Toyota
Institution:Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aobaya, Sendai 980-8578, Japan
Abstract:An efficient approach for the synthesis of a fully functionalized perhydrobenzoe]indene, the BCD ring system of andrastins A-D, is described. The synthesis commences from (±)-Wieland-Miescher ketone and features a Ti(III)-induced radical cyclization as the central step.
Keywords:Ti(III)-induced radical cyclization  Andrastins  Protein farnesyltransferase inhibitor
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