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Organocatalytic regio-, diastereo- and enantioselective γ-additions of isoxazol-5(4<i>H</i>)-ones to β,γ-alkynyl-α-imino esters for the synthesis of axially chiral tetrasubstituted α-amino allenoates

Fushuai Li, Shuai Liang, Yepeng Luan, Xuling Chen, Hanhui Zhao, Anqi Huang, Pengfei Li, Wenjun Li

2021Organic Chemistry Frontiers55 citationsDOI

Abstract

The chiral phosphoric acid catalyzed regio-, diastereo- and enantioselective reaction of isoxazol-5(4<italic>H</italic>)-ones with β,γ-alkynyl-α-imino esters has been developed.

Topics & Concepts

Enantioselective synthesisChemistryPhosphoric acidCatalysisOrganic chemistryStereochemistryCombinatorial chemistryAsymmetric Synthesis and CatalysisAxial and Atropisomeric Chirality SynthesisCyclopropane Reaction Mechanisms
Organocatalytic regio-, diastereo- and enantioselective γ-additions of isoxazol-5(4<i>H</i>)-ones to β,γ-alkynyl-α-imino esters for the synthesis of axially chiral tetrasubstituted α-amino allenoates | Litcius