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19
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0007442817
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note
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[6b]) was tested to give the product [PhCH= CH-CH(Ph)Me] in 86% yield.
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20
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0007354760
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note
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[7]
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21
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0007354098
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note
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The original phenylborate prepared from 12a and MeLi gave a 57:43 mixture of 11a and 3 under the best conditions (Table 1, Entry 4).
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22
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0007354222
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note
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1H NMR spectra, see Experimental Section).
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23
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0033553112
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Recently, Trost reported a palladium-catalyzed allylic coupling reaction involving the palladium enolate: B. M. Trost, F. D. Toste, J. Am. Chem. Soc. 1999, 121, 3543-3544.
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Trost, B.M.1
Toste, F.D.2
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0007398059
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note
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1H NMR spectroscopic data of the protons for α-Ar isomers of 11b-e were as follows. - Isomer of 11b: δ = 3.34 (dd, J = 12, 4 Hz, 1 H). - Isomer of 11c: δ = 3.33 (dd, J = 11, 4 Hz, 1 H). - Isomer of 11d: δ = 3.42 (dd, J = 12, 4 Hz, 1 H), - Isomer of 11c: δ = 3.28 (dd, J = 13, 4 Hz, 1 H).
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26
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0001547002
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T. Hayashi, M. Konishi, K. Yokota, M. Kumada, Chem. Lett. 1980, 767-768.
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Kumada, M.4
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