Iron(II)-catalyzed enantioselective meso-epoxide-opening with anilines

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Iron(II)-catalyzed enantioselective meso-epoxide-opening with anilines.

A highly enantioselective method for the catalytic opening of aromatic meso-epoxides with aniline derivatives was developed. The desired chiral β-amino alcohols were obtained in mostly good to very good yields with excellent enantioselectivities. Structural evidence of the pre-catalyst revealed a scarcely disclosed heptadentate Fe(II) complex with the chiral bipyridine ligand.

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Highly enantioselective iron(II)-catalyzed opening reaction of aromatic meso-epoxides with indoles.

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Rhodium-catalyzed regio- and enantioselective amination of racemic secondary allylic trichloroacetimidates with N-methyl anilines.

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ژورنال

عنوان ژورنال: Chemical Communications

سال: 2012

ISSN: 1359-7345,1364-548X

DOI: 10.1039/c2cc18032d