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Catalytic asymmetric total synthesis of diazabicyclooctane β-lactamase inhibitors avibactam and relebactam.

Zhi YangYu ChenLinxi WanXiangling CenPei TangXiangtao Chen
Published in: Chemical communications (Cambridge, England) (2022)
A catalytic asymmetric total synthesis of avibactam and relebactam, two marketed diazabicyclooctane (DBO) β-lactamase inhibitors (BLIs), has been accomplished. An important feature of this study is the creation of a stereogenic center by using Rh-catalysed asymmetric hydrogenation, affording the crucial α-amino acid ester derivative with high-level enantiocontrol (99% ee). Furthermore, the adoption of flow technologies for the assembly of a majority of intermediates significantly achieves a faster preparation and greater synthetic efficiency than corresponding batch procedures.
Keyphrases
  • klebsiella pneumoniae
  • gram negative
  • escherichia coli
  • multidrug resistant
  • amino acid
  • solid state
  • machine learning
  • crystal structure
  • deep learning
  • electronic health record
  • molecularly imprinted