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Copper-catalyzed regio- and enantioselective hydroamination of alkenes with hydroxylamines. | LitMetric

Copper-catalyzed regio- and enantioselective hydroamination of alkenes with hydroxylamines.

Angew Chem Int Ed Engl

Worldwide Medicinal Chemistry, Pfizer, Inc. Eastern Point Rd., Groton, CT 06340 (USA).

Published: February 2014

AI Article Synopsis

  • The catalytic hydroamination of alkenes with amines can efficiently produce valuable chiral amines from basic starting materials.
  • Mild copper-catalyzed methods are emphasized for the targeted synthesis of both straight-chain and branched chiral amines.
  • This approach offers a promising strategy for creating complex molecules in a straightforward manner.

Article Abstract

Adding value: The catalytic hydroamination of alkenes with amines holds promise to rapidly deliver value-added chiral amines from simple and accessible starting materials. The use of mild, Cu-catalyzed electrophilic amination strategies for the regioselective preparation of both linear and chiral branched amines is highlighted.

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Source
http://dx.doi.org/10.1002/anie.201309262DOI Listing

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