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Large boron ligands (i.e., tetraphenylethylene glycol) favor the axial orientation whereas small ligands (propanediol) favor the equatorial orientation. See
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77953104696
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With Lewis acids, the equatorial orientation is preferred. See
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With Lewis acids, the equatorial orientation is preferred. See
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3 has been claimed in Pd-catalyzed arylamination. See
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3 has been claimed in Pd-catalyzed arylamination. See
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3 complexes with Brønsted acids
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Consistent with this hypothesis, the borylative coupling reaction with tris(2,4-di- tert -butylphenyl) phosphite as the ligand (cone angle = 215°
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Consistent with this hypothesis, the borylative coupling reaction with tris(2,4-di- tert -butylphenyl) phosphite as the ligand (cone angle = 215°
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