Sequential hydrozirconation/Pd-catalyzed cross coupling of acyl chlorides towards conjugated (2E,4E)-dienones

Sequential hydrozirconation/Pd-catalyzed cross coupling of acyl chlorides towards conjugated (2E,4E)-dienones

Dienones are challenging building blocks in natural product synthesis due to their high reactivity and complex synthesis. Based on previous work and own initial results, a new stereospecific sequential hydrozirconation/Pd-catalyzed acylation of enynes with acyl chlorides towards conjugated (2E,4E)-d...

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Bibliographic Details
Main Authors: Benedikt Kolb, Daniela Silva dos Santos, Sanja Krause, Anna Zens, Sabine Laschat
Format: Article
Language:English
Published: Beilstein-Institut 2023-02-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
cross coupling
hydrozirconation
palladium catalysis
schwartz's reagent
terpenes
Online Access:https://doi.org/10.3762/bjoc.19.17

Internet

https://doi.org/10.3762/bjoc.19.17

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