Publication | Closed Access
Metal‐Free Enantioselective Electrophilic Activation of Allenamides: Stereoselective Dearomatization of Indoles
142
Citations
67
References
2014
Year
Stereoselective DearomatizationNovel OrganocatalystsEngineering3,3-Disubstituted Indolenine CoresOrganic ChemistryElectrophilic ActivationCatalysisNew Synthetic ShortcutChemistryStereoselective SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The effective and unprecedented chiral BINOL phosphoric acid catalyzed (1-10 mol%) dearomatization of indoles through electrophilic activation of allenamides (ee up to 94%), is documented. Besides the synthesis of 3,3-disubstituted indolenine cores, a dearomatization/hydrogen transfer cascade sequence is also presented as a new synthetic shortcut toward highly enantiomerically enriched indolines.
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