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Diastereoselective syntheses of chroman spiroketals via [4 + 2] cycloaddition of enol ethers and o-quinone methides
Authors:Marsini Maurice A  Huang Yaodong  Lindsey Christopher C  Wu Kun-Liang  Pettus Thomas R R
Affiliation:Department of Chemistry and Biochemistry, University of California at Santa Barbara Santa Barbara, California 93106-9510, USA.
Abstract:A variety of chroman spiroketals are synthesized via inverse-demand [4 + 2] cycloaddition of enol ethers and ortho-quinone methides (o-QMs). Low temperature o-QM generation in situ allows for the kinetic, diastereoselective construction of these motifs, providing entry to a number of unusual chroman spiroketal natural products.
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