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- W3008322011 endingPage "7088" @default.
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- W3008322011 abstract "The catalytic diastereodivergent construction of stereoisomers having two or more stereogenic centers has been extensively studied. In contrast, the switchable introduction of another stereogenic element, that is, Z/E configuration involving a polysubstituted alkene group, into the optically active stereoisomers, has not been recognized yet. Disclosed here is the pseudo-stereodivergent synthesis of highly enantioenriched tetrasubstituted alkene architectures from isatin-based Morita-Baylis-Hillman carbonates and allylic derivatives, under the cooperative catalysis of a tertiary amine and a chiral iridium complex. The success of the switchable construction of the tetrasubstituted alkene motif relies on the diastereodivergent 1,3-oxo-allylation reaction between N-allylic ylides and chiral π-allyliridium complex intermediates by ligand and substrate control, followed by the stereoselective concerted 3,3-Cope rearrangement process." @default.
- W3008322011 created "2020-03-06" @default.
- W3008322011 creator A5009884297 @default.
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- W3008322011 creator A5032330899 @default.
- W3008322011 creator A5040284332 @default.
- W3008322011 creator A5082556661 @default.
- W3008322011 date "2020-04-27" @default.
- W3008322011 modified "2023-10-18" @default.
- W3008322011 title "Pseudo-Stereodivergent Synthesis of Enantioenriched Tetrasubstituted Alkenes by Cascade 1,3-Oxo-Allylation/Cope Rearrangement." @default.
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- W3008322011 doi "https://doi.org/10.1002/anie.202000044" @default.
- W3008322011 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32073203" @default.
- W3008322011 hasPublicationYear "2020" @default.
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