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This is true despite some early developments in the field originating from the observation of α-arylated products when Pd-catalyzed cross-coupling reactions were conducted in acetone solvent (see ref 1c).
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This is true despite some early developments in the field originating from the observation of α-arylated products when Pd-catalyzed cross-coupling reactions were conducted in acetone solvent (see ref 1c).
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3 proved to be unsuccessful in promoting the reaction, and LiHMDS and NaOtBu provided intractable product mixtures in which negligible amounts of 2a were observed by use of GC.
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3 proved to be unsuccessful in promoting the reaction, and LiHMDS and NaOtBu provided intractable product mixtures in which negligible amounts of 2a were observed by use of GC.
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In neat acetone, L11 also provided good results for arylation with 1a (94% conv., 93% yield at 60 °C in 19 h).
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In neat acetone, L11 also provided good results for arylation with 1a (94% conv., 93% yield at 60 °C in 19 h).
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The use of 3-(trifluoromethyl)phenyl tosylate resulted in the formation the corresponding phenol as the major product under the standard conditions.
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The use of 3-(trifluoromethyl)phenyl tosylate resulted in the formation the corresponding phenol as the major product under the standard conditions.
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35
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See the Supporting Information.
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See the Supporting Information.
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Preliminary studies also showed that L13 was capable of cross-coupling electron-rich aryl bromides (4-bromotoluene and 4-bromoanisole) under similar conditions.
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Preliminary studies also showed that L13 was capable of cross-coupling electron-rich aryl bromides (4-bromotoluene and 4-bromoanisole) under similar conditions.
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