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78449313741
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33846918696
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Kakiuchi, F.1
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77953892735
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For synthesis of monoarylated aromatic ketones by ortho C-H arylation, see:;,. See also ref 7a
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For synthesis of monoarylated aromatic ketones by ortho C-H arylation, see: Gandeepan, P.; Parthasarathy, K.; Cheng, C.-H. J. Am. Chem. Soc. 2010, 132, 8569. See also ref 7a.
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Gandeepan, P.1
Parthasarathy, K.2
Cheng, C.-H.3
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78449297831
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Yields of 4 and 5 described in this paper are calculated based on the amounts of arylboronates 2, which were used as limiting reagents
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Yields of 4 and 5 described in this paper are calculated based on the amounts of arylboronates 2, which were used as limiting reagents.
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0001818455
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Kakiuchi, F.; Sekine, S.; Tanaka, Y.; Kamatani, A.; Sonoda, M.; Chatani, N.; Murai, S. Bull. Chem. Soc. Jpn. 1995, 68, 62
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Kakiuchi, F.1
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Tanaka, Y.3
Kamatani, A.4
Sonoda, M.5
Chatani, N.6
Murai, S.7
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36
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78449278081
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On the basis of GC analyses, more than 10% of 6 was used for the C-H alkylation for entries 3-8 of Table 1
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On the basis of GC analyses, more than 10% of 6 was used for the C-H alkylation for entries 3-8 of Table 1.
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37
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78449290284
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The C-H arylation of the monoarylation product is much slower than the diarylation of acetophenone in the absence of styrene. Therefore, it is likely that most of the diarylation product is formed directly from acetophenone without dissociating from the ruthenium center as the monoarylation product
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The C-H arylation of the monoarylation product is much slower than the diarylation of acetophenone in the absence of styrene. Therefore, it is likely that most of the diarylation product is formed directly from acetophenone without dissociating from the ruthenium center as the monoarylation product.
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