M.-L. Yao et al. / Tetrahedron 68 (2012) 3738e3743
3743
was stirred at 80 ꢀC for the appropriate time (Table 3) and then
diluted with 10 mL of ether. The aqueous layer was extracted twice
with ether (5 mL) and the combined organic phase was dried over
anhydrous Na2SO4. After evaporation of the solvent the residue was
purified by silica gel column chromatography [elute: hexane (or
pentane)dethyl acetate (or Et2O)]. The 1H NMR and 13C NMR
spectra of known compounds (11a),9e (11b),61 (11c),62 (11d),9e
(11f),63 (11g),64 (11h),9e (11i)9j are consistent with literature values.
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Acknowledgements
Financial support from the U.S. Department of Energy (gs1) and
the Robert H. Cole Foundation (gs2) is acknowledged. We also
thank Frontier Scientific for providing organoboronic acids and
organotrifluoroborate precursors.
Supplementary data
25. Yao, M.-L.; Reddy, M. S.; Zeng, W.; Hall, K.; Walfish, I.; Kabalka, G. W. J. Org.
Chem. 2009, 74, 1385.
Procedures for synthesis and characterization of products (1H
and 13C NMR spectra). Supplementary data related to this article
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