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Yamamoto, H, Oshima, K, Eds, Wiley-VCH: Weinheim, Germany
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Ogawa, A.1
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Under phosphine-free Pd-catalyzed hydrothiolation, internai alkynes were also active. See refs 2a and 2c. Recently, Ni-catalyzed thioailylation of terminal and internai alkynes with allyl phenyl sulfide have been reported. See: Hua, R.; Takeda, H.; Onozawa, S-y.; Abe, Y.; Tanaka, M. Org. Lett. 2007, 9, 263.
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Under phosphine-free Pd-catalyzed hydrothiolation, internai alkynes were also active. See refs 2a and 2c. Recently, Ni-catalyzed thioailylation of terminal and internai alkynes with allyl phenyl sulfide have been reported. See: Hua, R.; Takeda, H.; Onozawa, S-y.; Abe, Y.; Tanaka, M. Org. Lett. 2007, 9, 263.
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38349090097
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Crystal data for 3a: space group PĪ (no. 2) with a, 9.7203(4) Å, b, 9.7299(3) Å, c, 11.1909(4) Å, α, 98.111(1)°, β, 100.675(1)°, γ, 106.8189(9)°, Z, 2, p, 1.229 g/cm3, R, 0.061, and Rw, 0.172. See the Supporting Informaion for crystal data for 3b and 3c
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3, R = 0.061, and Rw = 0.172. See the Supporting Informaion for crystal data for 3b and 3c.
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2. Kuniyasu, H.; Yamashita, F.; Terao, J.; Kambe, N. Angew. Chem., Int. Ed. 2007, 46, 5929.
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2. Kuniyasu, H.; Yamashita, F.; Terao, J.; Kambe, N. Angew. Chem., Int. Ed. 2007, 46, 5929.
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3, R = 0.044, and Rw = 0.118.
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3, R = 0.044, and Rw = 0.118.
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