Phosphite dehydrogenase (PTDH) catalyzes the NAD(+)-dependent oxidation of phosphite to phosphate. This reaction requires the deprotonation of a water nucleophile for attack on phosphite. A crystal structure was recently solved that identified Arg301 as a potential base given its proximity and orientation to the substrates and a water molecule within the active site. Mutants of this residue sho...

In the soil there exist cycles of biological oxidation and reduction for inorganic compounds of sulfur and nitrogen. We have been interested in the possibility that a similar cycle might exist for inorganic compounds of phosphorus. In particular, we have been interested in one step of such a cycle, that of biological oxidation of orthophosphite to orthophosphate. There are few reports in the li...

The mol-ecule of the title compound, C(22)H(42)Si(2), lies on a center of inversion, and the triisopropyl-silyl groups are staggered.

The reaction of 3-mercapto-6-methyl-1, 2, 4-triazin-5 (2H)-one 1 with dimethyl 2a and trimethyl phosphite 3a at 100 C in absence of solvent yields the dimeric product 4 and while the alkylated products 5 and 6 are obtained for reaction with 3a. Methylation of 1 by methyl iodide gives alkylated product 5. Reaction of 1 with diethyl 2b and triethyl phosphite 3b by the same previous conditions yie...

To date the majority of work on the systemic fungicide phosphite (phosphonate) to control Phytophthora diseases has been conducted on horticultural crops. There is a paucity of work on the control of Phytophthora root and collar rots in natural plant communities. This paper gives an overview of studies conducted in Western Australia which examine the potential of using phosphite in plant commun...

Plant growth promoting rhizobacteria (PGPR) are potential agents to control plant pathogens and their combined use with biopesticides such as phosphites may constitute a novel strategy to incorporate in disease management programs. In the present study, 11 bacterial isolates were selected on the basis of their antagonistic activity against Macrophomina phaseolina in dual-culture tests, and thei...

A highly efficient, two-step sequence method for the deoxygenation of hydroxyl groups has been developed. The method involves the preparation of the 2-(2-iodophenyl)ethyl methyl phosphite derivative of an alcohol using methyl dichlorophosphite and 2-(2-iodophenyl)ethanol. Treatment of the phosphite intermediate with (n-Bu)3SnH/AIBN in refluxing benzene cleanly produces the deoxygenation product...

A simple and efficient one pot synthesis of 2-amino-4H-chromen-4-yl phosphonate derivatives has been accomplished by the condensation of salicylaldehyde, malononitrile/ethylcyanoacetate and triethyl phosphite/trimethyl phosphite in the presence of molecular iodine as catalyst in water at room temperature. All the reactions were very clean and the products were obtained in very good to excellent...

The structure of cerium(IV) bis-(phosphite), Ce(HPO3)2, has been solved by single-crystal X-ray diffraction and has trigonal (P-3m1) symmetry. The cerium(IV) cation exhibits site symmetry -3m. and is octa-hedrally coordinated by O atoms of the phosphite ligands (point group symmetry 3m.). The highly symmetrical compound has a layered structure parallel to the ab plane, and is closely related to...

Chiral gold(i) phosphite complexes are readily prepared modularly from 3,3'-bis(triphenylsilyl)-1,1'-bi-2-naphthol. These chiral gold(i) phosphite complexes are very reactive precatalysts for the [4+2] cycloaddition of aryl-substituted 1,6-enynes with enantiomeric ratios ranging from 86 : 14 up to 94 : 6.