4.7 Article

Expanding dynamic kinetic protocols: transaminase-catalyzed synthesis of α-substituted β-amino ester derivatives

Journal

CHEMICAL COMMUNICATIONS
Volume 49, Issue 91, Pages 10688-10690

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc46760k

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Funding

  1. Principado de Asturias
  2. Spanish MICINN
  3. MICINN [MICINN-12-CTQ2011-24237]

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Several alpha-alkylated beta-amino esters have been obtained via DKR processes employing a kit of transaminases and isopropylamine as an amino donor in aqueous medium under mild conditions. Thus, while acyclic alpha-alkyl-beta-keto esters afforded excellent conversions and enantioselectivities, although usually low diastereoselectivities, using more constrained cyclic beta-keto esters high to excellent inductions were obtained.

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