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[2a]
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A part of this work was presented at 43rd Symposium on the Chemistry of Natural Products, Osaka, 2001: Y. Yokoyama, H. Hikawa, M. Mitsuhashi, A. Uyama, M. Hiroki, M. Murakami, 43rd Tennen Yuki Kagoubutu Toronkai Koen Yoshisyu (Abstracts Paper) 2001, 539-544.
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A part of this work was presented at 43rd Symposium on the Chemistry of Natural Products, Osaka, 2001: Y. Yokoyama, H. Hikawa, M. Mitsuhashi, A. Uyama, M. Hiroki, M. Murakami, 43rd Tennen Yuki Kagoubutu Toronkai Koen Yoshisyu (Abstracts Paper) 2001, 539-544.
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40
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34547198583
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2O at 100°C for 3 h.
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2O at 100°C for 3 h.
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42
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0001379168
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It was reported that 2-iodo-N-allylaniline gave 3-methylindole (32) by intramolecular Heck reaction using these conditions; a) R. Odle, ; B. Blevins; M. Ratcliff; L. S. Hegedus, J. Org. Chem. 1980, 45, 2709-2710;
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It was reported that 2-iodo-N-allylaniline gave 3-methylindole (32) by intramolecular Heck reaction using these conditions; a) R. Odle, ; B. Blevins; M. Ratcliff; L. S. Hegedus, J. Org. Chem. 1980, 45, 2709-2710;
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44
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34547196533
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2 and TPPTS were further added to the mixture from the first reaction, and then aqueous AcOH was added for neutralization. However, the reaction did not proceed.
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2 and TPPTS were further added to the mixture from the first reaction, and then aqueous AcOH was added for neutralization. However, the reaction did not proceed.
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