Organic compounds reaction intermediates

Organozinc addition reactions to unsaturated systems lead to an intermediate zinc compound which is in most cases further hydrolyzed to give the corresponding protonated organic compound. This intermediate can also be trapped by reaction with electrophiles (see Electrophile) (E+) such as aldehydes, acyl chlorides, organic halides, silyl halides, and so on. Depending on the nature of the electrophile (see... 

AH of the commercial inorganic peroxo compounds except hydrogen peroxide are described herein, as are those commercial organic oxidation reactions that are beheved to proceed via inorganic peroxo intermediates. Ozonides and superoxides are also included, but not the dioxygen complexes of the transition metals. 

RTIX2 derivatives are covalent compounds, generally soluble in organic solvents. The aryl and vinyl derivatives are more stable than the corresponding alkyl compounds. This type of compound has been postulated to be an intermediate in many organic synthetic reactions involving thaUium(III) species. 

Hydrazine and its derivatives find considerable use in the synthesis of biologically active materials, dyestuff intermediates and other organic derivatives. Reactions of aldehydes to form hydrazides (RCH=NNH2) and azines (RCH=NN=CHR) are well known in organic chemistry, as is the use of hydrazine and its derivatives in the synthesis of heterocyclic compounds. 

As in the case of ceric and vanadium ions, the reaction of organic compounds with Co(III) proceeds via formation of an intermediate complex. Such a complex decomposes and produces free radicals capable of initiating vinyl polymerization. However, only a few reports on Co(IIl) ion-initiated grafting onto cellulose fibers are available [38]. 

The formation of isomeric aldehydes is caused by cobalt organic intermediates, which are formed by the reaction of the olefin with the cobalt carbonyl catalyst. These cobalt organic compounds isomerize rapidly into a mixture of isomer position cobalt organic compounds. The primary cobalt organic compound, carrying a terminal fixed metal atom, is thermodynamically more stable than the isomeric internal secondary cobalt organic compounds. Due to the less steric hindrance of the terminal isomers their further reaction in the catalytic cycle is favored. Therefore in the hydroformylation of an olefin the unbranched aldehyde is the main reaction product, independent of the position of the double bond in the olefinic educt ( contrathermodynamic olefin isomerization) [49]. 

It has been known from the earliest observations in gold chemistry that olefins form very weak 7r-complexes with gold in any of its oxidation states.1-3 Therefore, only a very few stable complexes of this type have been isolated. However, unstable 7r-complexes of olefins with gold compounds are believed to be important intermediates or transient species in gold-catalyzed reactions of unsaturated organic compounds.122-125,131,286-288,307-312... 

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