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3N as base and an equimolar amount of copper and palladium catalysts (0.01 equiv). When the coupling reaction was performed with diiodoanisole 5e, only 1 equiv of propargyl alcohol was used in the preparation.
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41
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0000035972
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The Wittig reaction of ylide 8 with the aldehydes affords the 3-E-alkylidene-succinic acid monoalkyl esters in a highly stereoselective way; for previous studies on this reaction see: (a) Paquette, L. A.; Schulze, M. M.; Bolin, D. J. Org. Chem. 1994, 59, 2043. (b) Röder, E.; Krauss, H. Liebigs Ann. Chem. 1992, 177.
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The Wittig reaction of ylide 8 with the aldehydes affords the 3-E-alkylidene-succinic acid monoalkyl esters in a highly stereoselective way; for previous studies on this reaction see: (a) Paquette, L. A.; Schulze, M. M.; Bolin, D. J. Org. Chem. 1994, 59, 2043. (b) Röder, E.; Krauss, H. Liebigs Ann. Chem. 1992, 177.
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4) and concentrated under reduced pressure. The residue was purified by chromatography and crystallization to give phenol derivatives 4a-f.
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