Chemoenzymatic preparation of fluorine-substituted β-lactam enantiomers exploiting Burkholderia cepacia lipase
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference17 articles.
1. β-Lactam Derivatives as Inhibitors of Human Cytomegalovirus Protease
2. β-Lactams in the New Millennium. Part-I: Monobactams and Carbapenems
3. β-Lactams in the New Millennium. Part-II: Cephems, Oxacephems, Penams and Sulbactam
4. Asymmetric Synthesis of β-Lactams by Staudinger Ketene-Imine Cycloaddition Reaction
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1. Chemoenzymatic enantioselective route to get (+) and (−) 4-acetoxy-azetidin-2-one by lipase-catalysed kinetic resolution and their applications;Bioorganic Chemistry;2022-03
2. Chiral β-lactam-based integrin ligands through Lipase-catalysed kinetic resolution and their enantioselective receptor response;Bioorganic Chemistry;2019-07
3. Burkholderia cepacia lipase: A versatile catalyst in synthesis reactions;Biotechnology and Bioengineering;2017-10-30
4. Enantio convergent biotransformation of O , O -dimethyl-4-oxoazetidin-2-ylphosphonate using fungal cells of Penicillium minioluteum and purified enzymes;Bioorganic Chemistry;2017-04
5. TheN-Hydroxymethyl Group as a Traceless Activating Group for the CAL-B-Catalysed Ring Cleavage of β-Lactams: A Type of Two-Step Cascade Reaction;European Journal of Organic Chemistry;2016-05
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