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tBuOH under an atmosphere of argon, and the reaction was allowed to stir at 30°C until complete. The reaction mixture was subjected to rotary evaporation, and the crude residue was purified by silica gel chromatography to give the cyclized product.
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For racemic syntheses of ricciocarpin A, see: (a) Eicher, T.; Massonne, K.; Herrmann, M. Synthesis 1991, 1173. (b) Ihara, M.; Suzuki, S.; Taniguchi, N. ; Fukumoto, K. J. Chem. Soc., Perkin Trans. 1 1993, 2251. (c) Ihara, M.; Suzuki, S.; Taniguchi, N.; Fukumoto, K. Chem. Commun. 1993, 755. (d) Takeda, K.; Ohkawa, N.; Hori, K.; Koizumi, T.; Yoshii, E. Heterocycles 1998, 47, 277.
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For racemic syntheses of ricciocarpin A, see: (a) Eicher, T.; Massonne, K.; Herrmann, M. Synthesis 1991, 1173. (b) Ihara, M.; Suzuki, S.; Taniguchi, N. ; Fukumoto, K. J. Chem. Soc., Perkin Trans. 1 1993, 2251. (c) Ihara, M.; Suzuki, S.; Taniguchi, N.; Fukumoto, K. Chem. Commun. 1993, 755. (d) Takeda, K.; Ohkawa, N.; Hori, K.; Koizumi, T.; Yoshii, E. Heterocycles 1998, 47, 277.
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0002462180
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For racemic syntheses of ricciocarpin A, see: (a) Eicher, T.; Massonne, K.; Herrmann, M. Synthesis 1991, 1173. (b) Ihara, M.; Suzuki, S.; Taniguchi, N. ; Fukumoto, K. J. Chem. Soc., Perkin Trans. 1 1993, 2251. (c) Ihara, M.; Suzuki, S.; Taniguchi, N.; Fukumoto, K. Chem. Commun. 1993, 755. (d) Takeda, K.; Ohkawa, N.; Hori, K.; Koizumi, T.; Yoshii, E. Heterocycles 1998, 47, 277.
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24
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0000617706
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For racemic syntheses of ricciocarpin A, see: (a) Eicher, T.; Massonne, K.; Herrmann, M. Synthesis 1991, 1173. (b) Ihara, M.; Suzuki, S.; Taniguchi, N. ; Fukumoto, K. J. Chem. Soc., Perkin Trans. 1 1993, 2251. (c) Ihara, M.; Suzuki, S.; Taniguchi, N.; Fukumoto, K. Chem. Commun. 1993, 755. (d) Takeda, K.; Ohkawa, N.; Hori, K.; Koizumi, T.; Yoshii, E. Heterocycles 1998, 47, 277.
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For an enantioselective syntheses of ricciocarpin A, see: Held, C.; Frohlich, R.; Metz, P. Angew. Chem., Int. Ed. 2001, 40, 1058.
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