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Copper-catalyzed asymmetric 1,6-conjugate addition of <i>in situ</i> generated <i>para</i>-quinone methides with β-ketoesters

Yi-Feng Wang, Chaojie Wang, Qing-Zhou Feng, Jing-Jing Zhai, Suo‐Suo Qi, Aiguo Zhong, Mingming Chu, Dan‐Qian Xu

2022Chemical Communications64 citationsDOI

Abstract

The first example of transition metal catalyzed asymmetric transformations of the in situ generated p -QMs has been developed, avoiding using pre-synthesized p -QMs requiring bulky 2,6-substitutions.

Topics & Concepts

StereocenterOxazolineChemistryConjugateIn situCatalysisQuinoneCopperMetalLewis acids and basesBrønsted–Lowry acid–base theoryCombinatorial chemistryEnantioselective synthesisStereochemistryOrganic chemistryMathematicsMathematical analysisSynthesis of Indole DerivativesChemical Synthesis and ReactionsAxial and Atropisomeric Chirality Synthesis
Copper-catalyzed asymmetric 1,6-conjugate addition of <i>in situ</i> generated <i>para</i>-quinone methides with β-ketoesters | Litcius