Oxidizing agents attachment

A number of l-aryl-2-thienylethylenes have been photocyclized in the presence of an oxidizing agent (usually iodine) to polycyclic aromatic compounds. Representative examples are given in Table 1. The mechanism, as with the conversion of stilbene to phenanthrene, probably involves conversion of the trans-alkene to the c/s-form, cyclization to the dihydro isomer, and oxidation of the latter to the fully aromatic compound. The yield of the cyclized product seems to decrease when the ethylene is attached to the /3-position of the thiophene. 

Dihydroxylation, the addition of two hydroxy groups across a C = C bond, converts fluorinated alkenes into different products depending on the presence or absence of a fluorine atom at the hydroxylated carbon. Partially fluorinated alkenes with vicinal hydrogen atoms attached to the C = C bond can be hydroxylated to vicinal diols. When the reaction is performed with a sufficiently strong oxidizing agent, the initially formed diols are oxidized to vicinal diketones as the end products. 

The reactivity of a terminal 1,13-diene with an interstitial deca(difluoromethylene) chain 1 is lower towards expoxidation with hypofluorous acid/acetonitrile complex21 due to the electron-withdrawing effect of the perfluoroalkyl chain attached directly to the C = C bond. The diepoxide 2 is obtained by repeated reaction with a very large excess of the oxidizing agent.21... 

The quinonemethide content of chemically modified lignins may be much higher. If quinonemethide precursors (—e.g. structures of type III) are present in high yield pulps in residues of condensed lignin attached to the fibers, attempts to bleach the pulps with oxidizing agents may lead... 

Sulfur has been used in linkers such as thioethers, sulfoxides, sulfones, sulfonic acids and their corresponding derivatives. A safety-catch linker for amines is based on 2-(thiobenzyl)ethylcarbamates [44]. Linkage is performed with preformed handles containing ethenyloxycarbonyl-protected amines 37. Attachment to thiomethyl-ated polystyrene 38 is performed under conditions involving radicals. Cleavage was performed with an oxidizing agent, which forms the retro Michael substrate (Scheme 6.1.11). 

PP/PA (polypropylene/polyallomer). These plastics are similar to polyethylene, but each unit of their chains has a methyl group attached. They are translucent, autoclavable, and have no known solvents at room temperature. They are slightly more susceptible than polyethylene to strong oxidizing agents. They offer the best stress-cracking resistance of the polyolefins. Products made of polypropylene are brittle at ambient temperature and may crack or break if dropped from benchtop height. 

In each of these complex ions there are six groups (water molecules and chloride ions) attached to the chromium ion. Chromic ion can be oxidized to chromate ion or dichromate ion by strong oxidizing agents, such as sodium peroxide in alkaline solution. 

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