Matches in SemOpenAlex for { <https://semopenalex.org/work/W2308291563> ?p ?o ?g. }
- W2308291563 endingPage "1499" @default.
- W2308291563 startingPage "1495" @default.
- W2308291563 abstract "Abstract New Schiff bases derived from chiral d ‐ camphor were determined to be effective phosphine ligands for the asymmetric palladium‐catalyzed allylic alkylation of activated methylene compounds, the allylic etherification of alcohols, and the allylic amination of primary amines or secondary amines, in which the corresponding products with various functional groups were achieved in good yields with excellent enantioselectivities (up to >99 % ee ). Remarkably, the palladium catalyst derived from Schiff base L2 afforded the highest level of enantioselectivity reported to date for allylic substitution reactions, including allylic etherification and allylic amination, which revealed the privileged role of d ‐camphor‐derived Schiff bases in palladium‐catalyzed allylic substitution reactions." @default.
- W2308291563 created "2016-06-24" @default.
- W2308291563 creator A5019478505 @default.
- W2308291563 creator A5028205204 @default.
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- W2308291563 creator A5054945722 @default.
- W2308291563 creator A5056483960 @default.
- W2308291563 creator A5073799726 @default.
- W2308291563 date "2016-03-22" @default.
- W2308291563 modified "2023-10-16" @default.
- W2308291563 title "A <scp>d</scp> -Camphor-Based Schiff Base as a Highly Efficient N,P Ligand for Enantioselective Palladium-Catalyzed Allylic Substitutions" @default.
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