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. 2003 Feb 20;5(4):595-8.
doi: 10.1021/ol0340179.

Probing electronic effects in the asymmetric Heck reaction with the BIPI ligands

Affiliations

Probing electronic effects in the asymmetric Heck reaction with the BIPI ligands

Carl A Busacca et al. Org Lett. .

Erratum in

  • Org Lett. 2003 May 1;5(9):1595

Abstract

[structure: see text] The new BIPI ligands are phosphinoimidazolines that can be electronically tuned in three different ligand regions to explore electronic effects in asymmetric catalysis. Their application to the asymmetric Heck reaction (AHR) in the creation of a chiral quaternary center is described. Enantioselectivity is shown for the first time to depend linearly on phosphine electron density. Changing the ligand basicity by variation of the R(2) or R(3) substituents reverses facial selectivity.

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