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

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

Journal Name: Letters in Organic Chemistry

Volume 2 , Issue 7 , 2005

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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.

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

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Article Details

VOLUME: 2
ISSUE: 7
Year: 2005
Page: [608 - 612]
Pages: 5
DOI: 10.2174/157017805774296993
Price: $65

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