Bicyclic Bridgehead Phosphoramidite (Briphos) Ligands with Tunable π-Acceptor Ability and Catalytic Activity in the Rhodium-Catalyzed Conjugate Additions

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A new type of bicyclic bridgehead phosphoramidites (briphos) is reported, where the geometrical constraints significantly enhance the π-acceptor ability compared with its monocyclic analogs. The briphos is shown to be highly efficient and tunable for Rh(I)-catalyzed conjugate additions of aryl boronic acids to α,β-unsaturated ketones and N-tosyl ketimines. (Chemical Equation Presented).
Publisher
AMER CHEMICAL SOC
Issue Date
2014-10
Language
English
Article Type
Article
Citation

ORGANIC LETTERS, v.16, no.20, pp.5490 - 5493

ISSN
1523-7060
DOI
10.1021/ol502772m
URI
http://hdl.handle.net/10203/193928
Appears in Collection
CH-Journal Papers(저널논문)
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