Anions oxyanionic groups

Common anions may be grouped as follows monatomic anions, oxyanions, and special anions. There are special endings for the first two groups the third group is small enough to be memorized. 

Phosphates are compoimds that contain oxyanions of phosphorus(V), ranging from the simple orthophosphate group to condensed chain, ring, and network anions. Oxyanions of phosphorus in lower oxidation states such as phosphite, HP03, are also known. 

Although a hydroxyl group strongly activates an aromatic ring toward electrophilic attack an oxyanion substituent is an even more powerful activator Electron delocaliza tion m phenoxide anion leads to increased electron density at the positions ortho and para to oxygen... 

In principle, numerous reports have detailed the possibility to modify an enzyme to carry out a different type of reaction than that of its attributed function, and the possibility to modify the cofactor of the enzyme has been well explored [8,10]. Recently, the possibility to directly observe reactions, normally not catalyzed by an enzyme when choosing a modified substrate, has been reported under the concept of catalytic promiscuity [9], a phenomenon that is believed to be involved in the appearance of new enzyme functions during the course of evolution [23]. A recent example of catalytic promiscuity of possible interest for novel biotransformations concerns the discovery that mutation of the nucleophilic serine residue in the active site of Candida antarctica lipase B produces a mutant (SerlOSAla) capable of efficiently catalyzing the Michael addition of acetyl acetone to methyl vinyl ketone [24]. The oxyanion hole is believed to be complex and activate the carbonyl group of the electrophile, while the histidine nucleophile takes care of generating the acetyl acetonate anion by deprotonation of the carbon (Figure 3.5). 

This section describes the nucleophilic reactions—acyl transfer reactions mostly—promoted by micelles and polysoaps. The nucleophiles are imidazoles, oxyanions and thiols, the same catalytic groups found ubiquitously in the enzyme active site. These nucleophiles are remarkably activated in the anionic form in the presence of cationic micelles and cationic polysoaps. These results are explained by the concept of the hydrophobic ion pair (Kunitake et al.,... 

As for all elements, the distribution of Mo in the environment depends critically on chemical speciation, including oxidation state (Bertine and Turekian 1973 Morford and Emerson 1999). However, Mo is somewhat unusual in both respects. In terms of ligand coordination. Mo is one of a small number of transition metals that commonly form oxy anions and coordinate only weakly with other environmentally common ligands such as Cl" or OH". Other such metals include Cr and W, which sit above and below Mo, respectively, in Group VI of the Periodic Table, as well as Tc, Re, Os and U. Hence, Mo chemistry has some analogies with these metals, as well as with nonmetals such as S, Se, P and As which also form oxyanions. 

Nitrobenzoylamino)-2,2-dimethylpropanamide (143 R = Me) reacts in methanol-DMSO solution with sodium methoxide to yield 5,5-dimethyl-2-(4-nitrophenyl)imidazol-4(5//)-one (144 R = Me). The 4-methoxyphenyl derivative and the parent phenyl derivative react similarly, as do compounds in which variation of the 2-substitutent (R = Pr , Ph, 4-O2NC6H4) was made. The mechanism of the cyclization probably involves initial formation of the anion of the alkanamide (145), which adds to the carbonyl group of the benzamido moiety to yield the tetrahedral oxyanion (146) proton transfer and dehydration then yield the heterocycle (144). The kinetics of hydrolysis in water at 70 °C and pH 2-11 of A-glycidylmorpholine (147) have been reported. ... 

Alkoxy(trisdimethylamino)phosphonium salts (PF6, C104 or BF4 as anions)765 are also used for the same purpose with good yields of course, alkoxy groups can be chosen as optically active451,766,767. Moreover, when the alkoxy chain is functionalized in the appropriate position by oxyanions, intramolecular etherification is made possible 3,6-anhydrohexosides were prepared in this way537 (reaction 232). 

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