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A step-economic and one-pot access to chiral C<sup>α</sup>-tetrasubstituted α-amino acid derivatives <i>via</i> a bicyclic imidazole-catalyzed direct enantioselective <i>C</i>-acylation

Mo Wang, Muxing Zhou, Lu Zhang, Zhenfeng Zhang, Wanbin Zhang

2020Chemical Science27 citationsDOIOpen Access PDF

Abstract

-tetrasubstituted α-amino acid derivatives with excellent enantioselectivities (up to 99% ee). This step-economic, one-pot, and auto-tandem strategy provides facile access to important chiral building blocks, such as peptides, serines, and oxazolines, which are often used in medicinal and synthetic chemistry.

Topics & Concepts

Enantioselective synthesisImidazoleBicyclic moleculeCatalysisChemistryAcylationStereochemistryCombinatorial chemistryOrganic chemistryAsymmetric Synthesis and CatalysisChemical Synthesis and AnalysisSynthesis and Catalytic Reactions
A step-economic and one-pot access to chiral C<sup>α</sup>-tetrasubstituted α-amino acid derivatives <i>via</i> a bicyclic imidazole-catalyzed direct enantioselective <i>C</i>-acylation | Litcius