Our research group first demonstrated that cationic rhodium (I) complexes with BINAP-type bisphosphine ligands are versatile new catalysts for highly chemo-, regio-, and enantioselective [2+2+2] cycloadditions. Highly efficient catalytic synthesis of substituted benzenes, cyclophanes, and nitrogen heterocycles was achieved with high chemo- and regioselectivity using these catalysts. Enantioselective variants of these cycloadditions were also developed, which realized efficient catalytic constructions of axial, planar, and central chirality.
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Tanaka et al. (2007) studied this question.
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