1999
DOI: 10.1007/pl00010269
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Chiral Binaphthyl Ligands with Buttressing Substituents

Abstract: Four macrocyclic and one non-cyclic chiral diphosphine ligand containing a 2,2 Hsubstituted 1,1 H -binaphthyl unit were synthesized in 6 steps from (R)-2,2 H -dimethoxy-1,1 H -binaphthyl in overall yields of 8±51%. Their asymmetric induction in allylic alkylation reactions was investigated showing enantioselectivities up to 98%.

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Cited by 2 publications
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“…L40e was the best chiral inductor in this case. The enantioselectivity strongly depends on the substrate nature since high enantioselectivities were obtained with rac- 1a whereas for rac- 1b and cyclic substrates rac- 3 , substrates with minor steric hindrance, the asymmetric induction was very low [ 89 ].…”
Section: Diphosphine Ligands In Asymmetric Allylic Alkylation Reacmentioning
confidence: 99%
“…L40e was the best chiral inductor in this case. The enantioselectivity strongly depends on the substrate nature since high enantioselectivities were obtained with rac- 1a whereas for rac- 1b and cyclic substrates rac- 3 , substrates with minor steric hindrance, the asymmetric induction was very low [ 89 ].…”
Section: Diphosphine Ligands In Asymmetric Allylic Alkylation Reacmentioning
confidence: 99%