Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes

Literature Information

Publication Date 2015-05-07
DOI 10.1039/C5QO00096C
Impact Factor 5.281
Authors

Feng Yu, Pinhong Chen, Guosheng Liu


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Abstract

A Pd-catalyzed intermolecular asymmetric hydroamination of styrenes was developed to give various chiral benzyl amides exclusively, in which the oxidation-stable pyridine-oxazoline was used as the chiral ligand to provide moderate to good enantioselectivities.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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