First stereoselective acylation of a primary diol possessing a prochiral quaternary center mediated by lipase TL from Pseudomonas stutzeri
Author:
Funder
Spanish MINECO
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference55 articles.
1. Enantioselective Synthesis of Oxygen-, Nitrogen- and Halogen-Substituted Quaternary Carbon Centers
2. Organocatalytic Formation of Quaternary Stereocenters
3. Metal-catalyzed asymmetric conjugate addition reaction: formation of quaternary stereocenters
4. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems
5. The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis
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1. On the Use of Orthoformates as an Efficient Approach to Enhance the Enzymatic Enantioselective Synthesis of (S)-Ibuprofen;Catalysts;2023-01-22
2. Biocatalysis at Extreme Temperatures: Enantioselective Synthesis of both Enantiomers of Mandelic Acid by Transesterification Catalyzed by a Thermophilic Lipase in Ionic Liquids at 120 °C;Catalysts;2020-09-14
3. Biotechnological potential of lipases from Pseudomonas: Sources, properties and applications;Process Biochemistry;2018-12
4. Biocatalytic Desymmetrization of Prochiral 3-Aryl and 3-Arylmethyl Glutaramides: Different Remote Substituent Effect on Catalytic Efficiency and Enantioselectivity;Advanced Synthesis & Catalysis;2018-10-22
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