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・ Phosphatidylinositol transfer protein
・ Phosphatidylinositol transfer protein, alpha
・ Phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase
・ Phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase
・ Phosphatidylinositol-3,4-bisphosphate 4-phosphatase
・ Phosphatidylinositol-3-phosphatase
・ Phosphatidylinositol-4,5-bisphosphate 3-kinase
・ Phosphatidylinositol-4,5-bisphosphate 4-phosphatase
・ Phosphatidylinositol-4-phosphate 3-kinase
・ Phosphatidylmyo-inositol mannosides
・ Phosphatidylserine
・ Phosphatidylserine decarboxylase
・ Phosphatocopida
・ Phosphatodraco
・ Phosphatosaurus
Phosphatrioxa-adamantane
・ Phosphaturic mesenchymal tumor
・ Phosphazene
・ Phosphene
・ Phosphene Dream
・ Phosphichthys
・ Phosphide
・ Phosphila
・ Phosphinate
・ Phosphine
・ Phosphine oxide
・ Phosphinidene
・ Phosphinimide ligands
・ Phosphinite
・ Phosphinoimidate


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Phosphatrioxa-adamantane : ウィキペディア英語版
Phosphatrioxa-adamantane

Phosphatrioxa-adamantane is an organophosphorus compound that is used as a precursor to bulky phosphine ligands.〔Paul G. Pringle, Martin B. Smith "Phosphatrioxa-adamantane Ligands" in Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, Edited by Paul C. J. Kamer and Piet W. N. M. van Leeuwen, 2012 John Wiley, New York. 〕 Abbreviated CgPH (for cage phosphine), it is a white solid.
The compound is prepared by the condensation of two equivalents of acetylacetone and phosphine:
:PH3 + 2 CH3C(O)CH2C(O)CH3 → HP(CH3CCH2CCH3)2O3 + H2O
The condensation is sometimes called the Buckler–Epstein reaction. Many diketones can be employed in place of acetylacetone. The P-H bond can be further derivitized, leading to a range of tertiary phosphines of potential value in homogeneous catalysis.
==References==


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