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Several solvent-free boratabenzene yttrium chlorides were synthesized and structurally characterized. Their reactions with KN(SiMe 3 ) 2 first gave boratabenzene yttrium amides; the latter reacted further with KN(SiMe 3 ) 2, which results in π-ligand displacement. The boratabenzene yttrium amides showed good catalytic activities for intramolecular hydroamination.
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Yuan et al. (2008) studied this question.
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