Diastereoselective Synthesis of 3-Phosphinoxido- and 3-Phosphono-1,2,3,4,5,6- Hexahydrophosphinine Oxides as Potential Precursors of Bidentate P-Ligands

Title: Diastereoselective Synthesis of 3-Phosphinoxido- and 3-Phosphono-1,2,3,4,5,6- Hexahydrophosphinine Oxides as Potential Precursors of Bidentate P-Ligands

Volume: 2 Issue: 7

Author(s): G. Keglevich, M. Sipos, V. Ujj and T. Kortvelyesi

Affiliation:

Keywords: p-heterocycles, michael-addition, hydrogenation, diastereoselectivity, bidentate p-ligand, chelate pt complex

Abstract: 1,2,3,4,5,6-Hexahydrophosphinine oxides with exocyclic P-function in position 3 can be obtained in a diastereoselective manner by the two-step conversion of 1,2-dihydrophosphinine oxides. Michael addition of the > P(O)H species on the α,β-double-bond of the starting P-cycle is followed by catalytic hydrogenation of the 1,2,3,6-tetrahydrophosphinine oxides so obtained. One of the bis(phosphine oxides) served, after deoxygenation, as a suitable bisphosphine ligand in complexation with PtCl2(PhCN)2. The different configuration of the ring P atom in the precursor and in the ligand suggested that the deoxygenation took place with inversion.

Cite this article as:

Keglevich G., Sipos M., Ujj V. and Kortvelyesi T., Diastereoselective Synthesis of 3-Phosphinoxido- and 3-Phosphono-1,2,3,4,5,6- Hexahydrophosphinine Oxides as Potential Precursors of Bidentate P-Ligands, Letters in Organic Chemistry 2005; 2 (7) . https://dx.doi.org/10.2174/157017805774296993