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Transition-metal derivatives carbon monoxide insertion into

Many transition metal alkyls react with carbon monoxide to give acyl compounds. In all these cases the acyl derivatives can be detected at least by infrared methods and in most cases isolated. Molybdenum, manganese, rhenium, iron, cobalt, rhodium, nickel, palladium, and platinum alkyls, Grignard reagents, and boranes, all react with carbon monoxide, and one can explain the products from these on the basis of carbon monoxide inserting into the metal alkyl. [Pg.208]

Figure C shows carbon monoxide insertion reactions. There are a number of reduction reactions of carbon monoxide catalyzed by transition metals, and these, I believe, all involve an insertion of carbon monoxide into a metal hydride as an initial step. Cobalt hydrocarbonyl reacts with carbon monoxide to give formate derivatives. This is probably an insertion reaction also. Figure C shows carbon monoxide insertion reactions. There are a number of reduction reactions of carbon monoxide catalyzed by transition metals, and these, I believe, all involve an insertion of carbon monoxide into a metal hydride as an initial step. Cobalt hydrocarbonyl reacts with carbon monoxide to give formate derivatives. This is probably an insertion reaction also.
The following discussion deals not only with this reaction, but related reactions in which a transition metal complex achieves the addition of carbon monoxide to an alkene or alkyne to yield carboxylic acids and their derivatives. These reactions take place either by the insertion of an alkene (or alkyne) into a metal-hydride bond (equation 1) or into a metal-carboxylate bond (equation 2) as the initial key step. Subsequent steps include carbonyl insertion reactions, metal-acyl hydrogenolysis or solvolysis and metal-carbon bond protonolysis. [Pg.913]

An interesting cyclization reaction was reported that involved the reaction of dienes, diynes, or ene-ynes with transition metals to form cyclopentenone derivatives in the presence of carbon monoxide.363 in a simple example, ene-yne 444 was heated with dicobalt octacarbonyl and CO to give a 68% yield of 445.364 jjjj transformation has become an important synthetic tool known as the Pauson-Khand reaction.365 jhe mechanism probably involves insertion of the alkene (or alkyne) into the transition metal bond, which is why it is presented in this section. Formally, it is a [2+2+l]-cycloaddition, but the accepted mechanism is the one proposed by Magnus,364 and shown in Figure 13.8.366 n has been stated that further study is required to... [Pg.1218]


See other pages where Transition-metal derivatives carbon monoxide insertion into is mentioned: [Pg.637]    [Pg.638]    [Pg.66]    [Pg.314]    [Pg.314]    [Pg.1416]    [Pg.314]    [Pg.76]    [Pg.905]    [Pg.76]    [Pg.50]    [Pg.60]    [Pg.597]    [Pg.598]    [Pg.7]    [Pg.1453]    [Pg.49]    [Pg.105]    [Pg.28]   
See also in sourсe #XX -- [ Pg.1453 , Pg.1454 , Pg.1455 , Pg.1456 , Pg.1457 ]




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Carbon insertion

Insertion into

Metal carbon monoxide

Metal insertion

Metal insertion transition metals

Metal inserts

Metal monoxides

Metallic derivates

Monoxide insertion

Transition metal monoxides

Transition metals insertion

Transition-metal derivatives

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