Synthesis of 1-methyl-2-diphenylphosphino-3-(1′-isoquinolyl)indole; an easily racemised ligand giving insights into catalytic asymmetric allylation
摘要:
The synthesis of the title compound is described, involving 2-lithiation and phosphinylation of the coupled heterocycle in the final step. Attempts to resolve the phosphine by previously described methods led to its immediate racemisation, also observed more slowly in the PdCl 2 complex, for which the X-ray structure is described. The phosphinamine formed a cationic Pd(1,3-diphenylallyl) complex with high diastereoselectivity. By analysis of the solution stucture using NMR techniques, in comparison with the X-ray structure, some inferences about the mechanism of allylic alkylation with related heterotopic ligands can be drawn.
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关键词:
N chelating ligand (pi-allyl)palladium complexes Allylic substitution Palladium complexes Chiral phosphine Mechanism 1-(2-diphenylphosphino-1-naphthyl)isoquinoline Resolution Hydroboration Isomerization
DOI:
10.1016/S0040-4020(97)00016-1
被引量:
年份:
1997
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