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- W4243379301 abstract "Eine fast perfekte palladiumkatalysierte kinetische Racematspaltung 1,3-disubstituierter unsymmetrischer Allylacetate nutzt Silylenolether als Nucleophile, um zu dem wichtigen 3-substituierten Furanon zu gelangen (siehe Schema; DACH=Diaminocyclohexyl, dba=Dibenzylidenaceton). Die Reaktion verläuft unter milden Bedingungen und liefert die gewünschten Produkte mit exzellenter Chemo-, Regio- und Enantioselektivität. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W4243379301 created "2022-05-12" @default.
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- W4243379301 creator A5090154587 @default.
- W4243379301 date "2012-02-16" @default.
- W4243379301 modified "2023-10-16" @default.
- W4243379301 title "Highly Enantioselective Synthesis of 3-Substituted Furanones by Palladium-Catalyzed Kinetic Resolution of Unsymmetrical Allyl Acetates" @default.
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