Highly enantioselective allylic amination reaction through aerobic oxidative organo-organo dual catalytic system

A variety of enantioenriched substituted imides were facilely synthesized through aerobic oxidation/allylic amination reactions of aldimines with MBH carbonates under N-heterocyclic carbene (NHC)/chiral tertiary amine dual catalysis. The strategy is attractive and valuable because of the convenient...

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Veröffentlicht in:New journal of chemistry 2024-04, Vol.48 (14), p.676-68
Hauptverfasser: Mou, Chengli, Liang, Guangping, Liang, Peiyao, Chen, Siyi, Wu, Chong, Teng, Shenghan, Wang, Shoulei
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Sprache:eng
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Zusammenfassung:A variety of enantioenriched substituted imides were facilely synthesized through aerobic oxidation/allylic amination reactions of aldimines with MBH carbonates under N-heterocyclic carbene (NHC)/chiral tertiary amine dual catalysis. The strategy is attractive and valuable because of the convenient one-step procedure, environmental friendliness, high enantioselectivity and good functional-group tolerance. An NHC/chiral tertiary amine dual catalytic system for the aerobic oxidation/allylic amination reaction has been developed. The combination of NHC with organo-catalysts especially with tertiary amine catalysts remains an underexplored area.
ISSN:1144-0546
1369-9261
DOI:10.1039/d4nj00478g