Phosphates isomerism

Further studies on 1,3-dipolar addition reactions of diazophosphonates have been recorded,122 and work on 2-diazo-l-hydroxyalkylphosphonates also continues.123 The ester (155 R = H) reacts with esters of acetylenedicarboxylic acid without liberation of nitrogen to give stereoisomeric C-phosphorylated pyrazolines, which can be decomposed with both phosphorus-carbon and carbon-carbon bond fission, affording mixtures containing dimethyl acetylphosphonate, dimethyl hydrogen phosphonate, and tri(alkoxycarbonyl)pyrazolines. In the reaction between the same diazophosphonate and diazomethane, the latter conceivably acts as a basic catalyst for proton transfer in a series of steps which includes phosphonate-phosphate isomerization. The importance of a labile proton is demonstrated by the fact that the ester (155 R = Me) does not react in the manner described above. 

Acid hydrolysis of cytidine ribitol pyrophosphate led to a series of products, depending on the conditions of hydrolysis. L-Ribitol 1-phosphate (n-ribitol 5-phosphate), isomeric ribitol phosphates formed by acid-catalyzed migration of the phosphate group from the terminal position, and 1,4-anhydro-DL-ribitol were isolated. 

In glycolysis, why must D-glucose-6-phosphate isomerize to D-fmctose-6-phosphate before the cleavage reaction with aldolase occurs (See p. 1026.)... 

In 1952, Perkow reported (242) that a-haloaldehydes did not react with trialkyl phosphites according to the Michaelis-Arbuzov reaction, although this had been repeatedly reported, but that a new type of reaction occurred, yielding dialkyl vinyl phosphates isomeric with the expected phosphonates. 

In a second reaction, glucose-l-phosphate isomerizes to give glucose-6-phosphate. 

Now, continuing with Figure 11.2, glyceraldehyde 3-phosphate isomerizes todihy-droxyacetone phosphate (Scheme 11.4). While this is simply the isomerization of an... 

Now, finally, sedoheptulose 7-phosphate undergoes a transketolase-catalyzed (EC 2.2.1.2) process (as in Scheme 11.7) to remove two carbon atoms using the enzyme cofactor thiamine diphosphate to yield ribose 5-phosphate and a two-carbon fragment that has remained attached to the thiamine cofactor of transketo-lase (EC 2.2.1.1, sedoheptulose 7-phosphate) (Scheme 11.11). When the two-carbon fragment is added to glyceraldehyde 3-phosphate, the material of Scheme 11.8 again is applied and xylulose 5-phosphate results. The xylulose 5-phosphate isomerizes to ribulose 5-phosphate as in Scheme 11.9 (with intervention of ribulose phosphate 3-epimerase (EC 5.1.3.1). And, the ribose 5-phosphate, an aldose, isomerizes (an aldose-ketose isomerase, EC 5.3.1.6, ribose 5-phosphate isomerase) to ribulose 5-phosphate. 

Efficient utilization of the fructose requires phosphorylation of the glyceraldehyde. Tracer experiments show that the carbon 1 of fructose appears as both carbons 1 and 6 of glucose. This is the result of triose phosphate isomerization followed by (conventional) aldolase condensation to hexose diphosphate. The conversion of fructose diphosphate to glucose-6-phosphate requires a phosphatase and an isomerase, as discussed in the pentose phosphate pathway. 

G. Alagona, P. Desmeules, C. Ghio, and P. A. Kollman, /. Am. Chem. Soc., 106, 3623 (1984). Quantum Mechanical and Molecular Mechanical Studies on a Model for the Dihy-droxyacetone Phosphate-Glyceraldehyde Phosphate Isomerization Catalyzed by Tiiose-phosphate Isomerase (TIM). 

Katz, J. Landau, B. R., and Barsch, G. E., 1966, Pentose cycle, triose phosphate isomerization and lipogenesis in rat adipose tissue, /. Biol. Chem. 241 727. 

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