Phosphorochloridates phosphorylation

When the monosodium salts of uracil and similar pyrimidines react with diphenyl phosphorochloridate, phosphorylation takes place on oxygen unless other suitable nucleophilic centres are present and free.69 The reaction between the sodium salt of a 1,3-dicarbonyl compound and diethyl phosphorochloridothionate yields the Z-vinylphosphorothionate if the tetrabutylammonium salt is employed, the product has E geometry. This phenomenon has been interpreted in terms of the shape of the... 

PHOSPHORYLATION 2-Chloromethyl-4-nitrophenyl phosphorochloridate. o-Phenyl-ene phosphorochloridate. Phosphoryl chloride. Phosphoryl chloride-Trimethyl phosphate. 

A glyceryl 2-aminoethylphosphonolipid has been isolated from Tetrahymenapyriformis and (45) has been detected by g.l.c.-mass spectrometry in both the lipid and proteinaceous fractions of human brain. The zwitterionic (45) was converted into volatile (46) by acetylation and methylation. Phosphonolipids derived from A-methyl-(45) have been synthesised by acetylation of A-methyl-(45) and subsequent conversion to the phosphorochloridate for the phosphorylation step. °... 

Chlorodiphenylphosphine 488 reacts with a-sulphinyl carbanions to give a-sulphinylphosphines 489 which undergo ready isomerization to a-sulphenylphosphine oxides 4W (equation 295). The report of Almog and Weissman that a-sulphinyl carbanions react with phosphorochloridates 491 to give a-phosphoryl sulphoxides 492 calls for correction (equation 296). Actually, the phosphorylation occurs at the oxygen atom of the ambident dimsyl anion, and is followed by the Pummerer-type reaction affording diethylphosphoric acid and tetraethyl pyrophosphate among other products . ... 

On pp. 45 and 57 we referred to the action of chlorine1 and of N-chlorosuccinimide2 on dialkyl phosphites producing dialkyl phosphorochloridates. We have made use of the latter in producing a variety of esters of orthophosphoric acid and of phos-phoramidates, and reference has already been made to many such reactions (p. 82). These processes are, in a sense, phosphorylations of the alcohols or of the amines respectively. 

Phosphate groups can also be removed by dissolving-metal reduction. Reductive removal of vinyl phosphate groups is one of the better methods for conversion of a carbonyl compound to an alkene.150 151 The required vinyl phosphate esters are obtained by phosphorylation of the enolate with diethyl phosphorochloridate or NJ, N, N -tetra-methyldiamidophosphorochloridate.152 153... 

Furthermore, this phosphorylation reaction could be applied not only to the glycosyl position but also to other hydroxyl groups. When compound 38 (Figure 11) was treated with butyl-lithium and diphenyl phosphorochloridate as above, a syrupy 4-phosphate 39 was obtained whose structure was unequivocally confirmed by 3oOMHz -NMR. A quartet signal of H-4 (6 4.70ppm,... 

After had been treated with one equivalent of butyllithium and then with dibenzyl phosphorochloridate as above, the mixture was hydrogenolyzed immediately. Of the two free hydroxyl groups in 3, the more acidic one on C-l was phosphorylated selectively. The desired 1-a-monophosphate was isolated after purification with a silica gel column (CHCl3-Me0H-H20 40 10 1) as its sodium salt (65% from ). 

In preparation for the eventual removal of the undesired oxygen function at C-10 of 313 via a Birch reduction, the phenol 313 was phosphorylated with diethyl phosphorochloridate in the presence of triethylamine to give 314, which underwent stereoselective reduction with sodium borohydride with concomitant N-deacylation to deliver the amino alcohol 315. N-Methylation of 315 by the Eschweiler-Clarke protocol using formaldehyde and formic acid followed by ammonolysis of the ester group and acetylation of the C-2 hydroxyl function afforded 316. Dehydration of the amide moiety in 316 with phosphorus oxychloride and subsequent reaction of the resulting amino nitrile 317 with LiAlH4 furnished 318, which underwent reduction with sodium in liquid ammonia to provide unnatural (+)-galanthamine. 

A synthetic approach to /3-sultams containing a direct bond between a tri- or tetracoordinated phosphorus atom and the nitrogen atom of the 1,2-thiazetidine 1,1-dioxide ring has been realized by direct phosphitylation or phosphorylation at nitrogen. Unfortunately, attempts to synthesize N-phosphorylated /3-sultams by reaction with diethyl phosphorochloridate and diethyl phosphorobromidate, generated in situ from diethyl phosphate and carbon tetrachloride or carbon tetrabromide, failed. However, when the /3-sultam is treated with freshly distilled diethyl phosphorochloridite or tetramethylphosphorodiamidous chloride in the presence of triethylamine, the expected AHliethy I phosphite and iV-phosphorodiamidous /3-sultams 150 are obtained (Equation 10). /3-Sultams unsubstituted... 

Diphenyl phosphorochloridate is one of the most widely employed phosphorylating reagents for the preparation of phosphomonoesters (Scheme 3.17a).94 The chloride acts as a leaving group that can be displaced by hydroxyls. The phenyl groups act as protecting groups that... 

Phosphorylation. Dibenzyl phosphorochloridate is widely used for phosphorylation of alcohols, but is more difficult to prepare than the fluoridate. Phenol is very readily phosphorylated by 1 and CsF in CH3CN, and indeed a phenolic hydroxyl group is selectively attacked even in the presence of a primary hydroxyl group. Primary and anomeric alcohols are preferentially phosphorylated in the presence of a secondary hydroxyl group. Alcohols that are insoluble in acetonitrile can be phosphorylated by 1 and DBU in place of CsF. 

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