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- W4377822015 abstract "The front cover picture illustrates that intramolecular [4+2] cycloaddition of a simply attained chiral allenecarboxanilide affords the pseudoenantiomeric alkenyl bromides shown, which can be readily functionalized to give diverse chiral “Himbert diene” ligands. The synthesis can be readily scaled to produce decagram quantities of ligands. These ligands match, or exceed, the performance of existing “best-in-class” chiral dienes over nine types of enantioselective Rh(I)-catalyzed 1,4-addition or 1,2-addition reactions. Details can be found in the Research Article by Simon Woodward, Hon Wai Lam and co-workers (R. K. Rit, H. Li, S. P. Argent, K. M. Wheelhouse, S. Woodward, H. W. Lam, Adv. Synth. Catal. 2023, 365, 1629–1639; DOI: 10.1002/adsc.202300039)." @default.
- W4377822015 created "2023-05-24" @default.
- W4377822015 date "2023-05-23" @default.
- W4377822015 modified "2023-10-17" @default.
- W4377822015 doi "https://doi.org/10.1002/adsc.v365.10" @default.
- W4377822015 hasPublicationYear "2023" @default.
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