Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids
Covering: up to the end of 2017 Enantioselective Pd-catalyzed allylic alkylations of prochiral enolates represent a powerful tool for the construction of all-carbon quaternary stereocenters. This review describes the emergence of such reactions as strategic linchpins that enable efficient, stereocon...
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Veröffentlicht in: | Natural product reports 2018-06, Vol.35 (6), p.559-574 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Covering: up to the end of 2017
Enantioselective Pd-catalyzed allylic alkylations of prochiral enolates represent a powerful tool for the construction of all-carbon quaternary stereocenters. This review describes the emergence of such reactions as strategic linchpins that enable efficient, stereocontrolled syntheses of
Aspidosperma
and related monoterpene indole alkaloids.
The development of new heterocyclic substrate classes for palladium-catalyzed allylic alkylation has enhanced synthetic access to structurally diverse monoterpene indole alkaloids. |
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ISSN: | 0265-0568 1460-4752 |
DOI: | 10.1039/c7np00069c |