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10
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0012151303
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note
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2RuCp*Cl] were ineffective for the propargylic substitution reaction.
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11
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0012152139
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note
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Unfortunately, no propargylic substitution reactions of 2a with alcohols, amines, acetone, and silyl enol ethers in the presence of 1e occurred under similar reaction conditions.
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12
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0012193373
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note
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In contrast to the reaction of 2.4-diphenyl-3-butyn-2-ol (2h) (Table 2, run 14), the reaction of 1,1,3-triphenyl-2-propyn-1-ol with "BuSH at 60 °C for 16 h afforded not the corresponding propargylic product but 1,3,3- triphenyl-2-propen-1-one in 80% yield as a sole product.
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13
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0012114329
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note
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12
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14
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0012113895
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note
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When -4a was treated with "BuSH at room temperature, racemic 5aa was formed.
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15
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0001120361
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0037032307
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2 and CpRuCl(cod) at 100 °C, but available substrates were strictly limited to the propargylic carbonates bearing an internal alkyne group: Kondo, T.; Kanda, Y.; Baba, A.; Fukuda, K.; Nakamura, A.; Wada, K.; Morisaki, Y.; Mitsudo, T. J. Am. Chem. Soc. 2002, 124, 12960.
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(a) Kondo, T.; Mitsudo, T. Chem. Rev. 2000, 100, 3205 and references therein.
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