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Stereodivergent Construction of Vicinal Acyclic Quaternary–Tertiary Carbon Stereocenters by Michael-Type Alkylation of α,α-Disubstituted <i>N</i>-<i>tert</i>-Butanesulfinyl Ketimines

Nuermaimaiti Yisimayili, Hui Liu, Yun Yao, Chong‐Dao Lu

2021Organic Letters24 citationsDOI

Abstract

Vicinal quaternary–tertiary carbon stereocenters were constructed with excellent stereoselectivity via aza-enolization of enantioenriched acyclic N-tert-butanesulfinyl ketimines bearing two sterically similar α-linear alkyl substituents followed by conjugate addition to nitroalkenes. Further changes of the absolute configuration of the sulfinyl group and/or the α-stereocenter in the ketimine allowed the facile stereodivergent synthesis of all four diastereomers of the Michael-type alkylation adducts. This reaction is a successful example of acyclic stereocontrol based on stereoselective α-deprotonation for the formation of fully substituted aza-enolates from ketone derivatives.

Topics & Concepts

StereocenterChemistryAlkylationDiastereomerMichael reactionStereoselectivityDeprotonationStereochemistryEnantioselective synthesisChiral auxiliaryKetoneOrganic chemistryCatalysisIonAsymmetric Synthesis and CatalysisAsymmetric Hydrogenation and CatalysisSynthetic Organic Chemistry Methods
Stereodivergent Construction of Vicinal Acyclic Quaternary–Tertiary Carbon Stereocenters by Michael-Type Alkylation of α,α-Disubstituted <i>N</i>-<i>tert</i>-Butanesulfinyl Ketimines | Litcius