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For the usefulness of phenol derivatives as synthetic intermediates, see:. Simaan S., Siegel J.S., and Biali S.E. J. Org. Chem. 68 (2003) 3699
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27744478089
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Our recent publications on the chemical transformations of Baylis-Hillman adducts, see:
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Our recent publications on the chemical transformations of Baylis-Hillman adducts, see:. Park D.Y., Lee M.J., Kim T.H., and Kim J.N. Tetrahedron Lett. 46 (2005) 8799
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Acetone dicarboxylate has been used as a three-carbon unit in many reactions, see:
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Acetone dicarboxylate has been used as a three-carbon unit in many reactions, see:. Chung J.Y.L., Cai C., McWilliams J.C., Reamer R.A., Dormer P.G., and Cvetovich R.J. J. Org. Chem. 70 (2005) 10342
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33746721780
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note
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3 (152 mg, 1.1 mmol) and heated to 50-60 °C for 5 h. After usual aqueous extractive workup and column chromatographic purification process (hexanes/ether, 15:1), we obtained 4a as a white solid, 154 mg (49%). The other compounds were synthesized analogously.
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34
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0037094004
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For the synthesis of 2,6-diarylphenol derivatives, see:
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For the synthesis of 2,6-diarylphenol derivatives, see:. Kano T., Ohyabu Y., Saito S., and Yamamoto H. J. Am. Chem. Soc. 124 (2002) 5365
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Yamamoto, H.4
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0033615324
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Saito S., Kano T., Muto H., Nakadai M., and Yamamoto H. J. Am. Chem. Soc. 121 (1999) 8943
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Saito, S.1
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Yamamoto, H.5
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36
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33746682191
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note
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4g,4h
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