| Literature DB >> 30138551 |
Julia F Hyslop1,2, Sarah L Lovelock2,3, Peter W Sutton4,5, Kristin K Brown6, Allan J B Watson7, Gheorghe-Doru Roiban2.
Abstract
N-Functionalized amino acids are important building blocks for the preparation of diverse bioactive molecules, including peptides. The development of sustainable manufacturing routes to chiral N-alkylated amino acids remains a significant challenge in the pharmaceutical and fine-chemical industries. Herein we report the discovery of a structurally diverse panel of biocatalysts which catalyze the asymmetric synthesis of N-alkyl amino acids through the reductive coupling of ketones and amines. Reactions have been performed on a gram scale to yield optically pure N-alkyl-functionalized products in high yields.Entities:
Keywords: N-methyl amino acid dehydrogenases; biocatalysis; ketimine reductases; reductive amination; α-keto amino acids
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Year: 2018 PMID: 30138551 DOI: 10.1002/anie.201806893
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336