4.7 Article

Synthesis of protected 3-aminopiperidine and 3-aminoazepane derivatives using enzyme cascades

期刊

CHEMICAL COMMUNICATIONS
卷 56, 期 57, 页码 7949-7952

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc02976a

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资金

  1. European Research Council [742987, 788231-ProgrES-ERC-2017-ADG]
  2. EU [737395]
  3. BBSRC [BB/M027791/1, BB/M02903411, BB/M028836/1]
  4. Industrial Biotechnology Innovation Centre (IBioIC)
  5. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/S010459/1]
  6. Prozomix Ltd.
  7. BBSRC [BB/M028836/1, BB/M027791/1, BB/S010459/1] Funding Source: UKRI
  8. EPSRC [EP/S01778X/1] Funding Source: UKRI

向作者/读者索取更多资源

Multi-enzyme cascades utilising variants of galactose oxidase and imine reductase led to the successful conversion ofN-Cbz-protectedl-ornithinol andl-lysinol tol-3-N-Cbz-aminopiperidine andl-3-N-Cbz-aminoazepane respectively, in up to 54% isolated yield. Streamlining the reactions into one-pot prevented potential racemisation of key labile intermediates and led to products with high enantiopurity.

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