Molecular Basis for the Enantioselective Ring Opening ofβ-Lactams Catalyzed byCandida antarctica Lipase B
Author:
Publisher
Wiley
Subject
General Chemistry
Cited by 52 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Use of Lipases as a Sustainable and Efficient Method for the Synthesis and Degradation of Polymers;Journal of Polymers and the Environment;2023-11-27
2. Selective Functionalizations of Cycloalkene‐Fused β‐Lactams and their Transformations into Densely‐Substituted Three‐Dimensional Molecular Entities;Asian Journal of Organic Chemistry;2023-11-10
3. Enzymatic Strategies for the Preparation of Pharmaceutically Important Amino Acids through Hydrolysis of Amino Carboxylic Esters and Lactams;Current Medicinal Chemistry;2022-12
4. Chemoenzymatic enantioselective route to get (+) and (−) 4-acetoxy-azetidin-2-one by lipase-catalysed kinetic resolution and their applications;Bioorganic Chemistry;2022-03
5. Beyond nylon 6: polyamides via ring opening polymerization of designer lactam monomers for biomedical applications;Chemical Society Reviews;2022
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