Matches in SemOpenAlex for { <https://semopenalex.org/work/W2931982432> ?p ?o ?g. }
- W2931982432 endingPage "6439" @default.
- W2931982432 startingPage "6435" @default.
- W2931982432 abstract "In the presence of a [Cp*RhCl2]2 catalyst, the Lewis acid In(OTf)3, and the mild base Na2CO3, aromatic carboxylates and α,β-unsaturated ketones undergo a unique hydroarylation/Claisen/retro-Claisen process to give the corresponding indanones. In this carboxylate-directed ortho-C−H annelation, the C−COR bond of the ketone and the CO−OH group of the aromatic carboxylate are cleaved, and the hydroxy group is transferred from the aromatic to the aliphatic acyl residue. This reactivity is synthetically useful, particularly when starting from cyclic ketones, which are converted into indanones bearing aliphatic carboxylate side chains, thus greatly increasing the molecular complexity of aromatic carboxylates in a single step." @default.
- W2931982432 created "2019-04-11" @default.
- W2931982432 creator A5007655609 @default.
- W2931982432 creator A5027184362 @default.
- W2931982432 creator A5059954532 @default.
- W2931982432 creator A5063027653 @default.
- W2931982432 creator A5079104664 @default.
- W2931982432 creator A5086344136 @default.
- W2931982432 date "2019-05-06" @default.
- W2931982432 modified "2023-10-11" @default.
- W2931982432 title "Rhodium‐Catalyzed Annelation of Benzoic Acids with α,β‐Unsaturated Ketones with Cleavage of C−H, CO−OH, and C−C Bonds" @default.
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