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Total Syntheses of Secalonic Acids A and D
Authors:Tian Qin  Prof. Dr. John A. Porco Jr.
Affiliation:Department of Chemistry and Center for Chemical Methodology and Library Development (CMLD‐BU), Boston University, 590 Commonwealth Avenue, Boston, MA 02215 (USA)
Abstract:Total syntheses of the dimeric tetrahydroxanthone natural products secalonic acids A and D are described. Key steps involve kinetic resolution of the tetrahydroxanthone core structure using homobenzotetramisole catalysis and late‐stage copper(I)‐mediated homodimerization of complex aryl stannane monomers.
Keywords:dimerization  kinetic resolution  natural products  stannanes  total synthesis
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