4.5 Article

Catalytic Enantioselective Synthesis of Azepine-Fused Planar-Chiral Ferrocenes by Pt-Catalyzed Cycloisomerization

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ORGANOMETALLICS
卷 38, 期 20, 页码 4029-4035

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AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.9b00422

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  1. Mitsubishi Material Corporation
  2. Waseda University

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Enantioselective synthesis of azepine-fused planarchiral ferrocenes was achieved by the chiral cationic Pt-catalyzed intramolecular cycloisomerization of N-propargyl-2-ferrocenylanilines. A mechanistic study using an N-allenyl analogue indicated that the reaction proceeded selectively in a 7-exo-dig manner along with isomerization of the exo-olefin moiety. A methanesulfonylamino tether was crucial for selective cycloisomerization. This is the first example of the enantioselective synthesis of heteropin-fused planarchiral ferrocenes.

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