Primary chelation

Of nutrient chelates in the human diet, oxalates and phytates are the most common. OxaUc acid (8), found principally in spinach, rhubarb leaves, beet leaves, some fmits, and mushrooms, is a primary chelator of calcium. Oxalate present in pineapple, kiwifmit, and possibly in other foods, occurs as calcium... 

Of nutrient chelates in the human diet, oxalates and phytules arc Ihe most common. Oxalic acid, found principally in spinach, rhubarb leaves, beet leaves, some fruits, and mushrooms, is u primary chelator of calcium. Oxalate present in pineapple, kiwifmil, and possibly in other foods, occurs as calcium oxalale. CaCiOj. This compound is in the form of needle-like crystals, known as raphidcs. which can produce painful sensations in the mouth when eaten raw. The effects of oxalic acid in the diet may he twofold. First, it forms strong chelates with dietary calcium, rendering the culcium unavailable for absorption and assimilation. Secondly, absorbed oxalic acid causes assimilated Ca to be precipitated as insoluble salts that accumulate in the renal glomeruli and contribute to the formation of renal calculi. 

Ion-exchange resins are categorized by the nature of functional groups attached to a polymeric matrix, by the chemistry of the particular polymer in the matrix, and by the porosity of the polymeric matrix. There are four primary types of functionaHty strong acid, weak acid, strong base, and weak base. Another type consists of less common stmctures in specialty resins such as those which have chelating characteristics. 

The ahphatic alkyleneamines are strong bases exhibiting behavior typical of simple aUphatic amines. Additionally, dependent on the location of the primary or secondary amino groups iu the alkyleneamines, ring formation with various reactants can occur. This same feature allows for metal ion complexation or chelation (1). The alkyleneamines are somewhat weaker bases than ahphatic amines and much stronger bases than ammonia as the piC values iadicate (Table 2). 

On the contrary, in the latter case, a total loss of stereoselectivity occurs68. TV-Bis-benzyl-a-amino aldehydes 1 (R = R3 = Bn) under the assistance of boron trifluoride, zinc bromide or tin(lV) chloride lead to the nonchclation-controlled adducts preferentially, whereas titanium(IV) chloride or magnesium bromide result in chelation control70. In some cases, the O-trimcthylsilyl cyanohydrins arc the primary products, but the workup procedure usually provides the desily-lated products. 

The primary mode of action of this class of antimycotics is interference with uptake and accumulation of products required for cell membrane synthesis. In higher concentrations it causes a disturbance of the cellular permeability. Some investigations show an interaction with Fe(M)- ions the compounds acting as chelators. Very high concentrations interfere with the function of fungal mitochondria. 

The primary reason for studying aqueous plutonium photochemistry has been the scientific value. No other aqueous metal system has such a wide range of chemistry four oxidation states can co-exist (III, IV, V, and VI), and the Pu(IV) state can form polymer material. Cation charges on these species range from 1 to 4, and there are molecular as well as metallic ions. A wide variety of anion and chelating complex chemistry applies to the respective oxidation states. Finally, all of this aqueous plutonium chemistry could be affected by the absorption of light, and perhaps new plutonium species could be discovered by photon excitation. 

Similar results were obtained using n-BuMgBr-CuCN and tertiary allylic acetates, although under these conditions there is competition from SN2 substitution with primary acetates.33 The stereoselectivity is reversed with a hydroxy group, indicating a switch to a chelated TS. 

These reactions exhibit excellent diastereoselectivity derived from the chiral oxazo-lidinone auxiliary. The Lewis acid forms a chelate with the oxazoline and presumably also serves to enhance reactivity. In addition to ethyl, other primary, secondary, and tertiary alkyl radicals, as well as acetyl and benzoyl radicals were used successfully in analogous reactions. 

Ligands with S donors in addition to N and or O donors bound to Co11 are reasonably large in number. For example, the 4-amino-3-alkyl-l,2,4-triazole-5-thione can bind Co11 as a chelate employing the primary amine and thione substituents on the five-membered ring,510 whereas the trifluoromethyl ligand (afmt) forms [Co(afmt)2(H20)2](N03)2, defined as the A -irons isomer... 

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