Oxidations to ketones

The attack of OH obeys the Markovnikov rule. Higher alkenes are oxidized to ketones and this unique oxidation of alkenes has extensive synthetic appli-cations[23]. The oxidation of propylene affords acetone. Propionaldehyde is... 

Secondary alcohols are oxidized to ketones by the same reagents that oxidize primary alcohols... 

FIGURE 18.20 NAD and NADP participate exclusively iii two-electroii transfer reactions. For example, alcohols can be oxidized to ketones or aldehydes via hydride transfer to NAD(P). ... 

Some alkyl substituents with a secondary benzylic carbon can be oxidized to ketones using KMn04 at 50 °C in water Eqqs. (35) and (36). In the case of the fluorene complex only, this oxidation could be alternatively achieved using aqueous... 

An alternative procedure for oxidation to ketones involves treatment of the alkylborane with a quaternary ammonium perruthenate salt and an amine oxide186 (see Entry 6 in Scheme 4.9). Use of dibromoborane-dimethyl sulfide for hydroboration of terminal alkenes, followed by hydrolysis and Cr(VI) oxidation gives carboxylic acids.187... 

Selective oxidations are possible for certain bicyclic hydrocarbons.285 Here, the bridgehead position is the preferred site of initial attack because of the order of reactivity of C—H bonds, which is 3° > 2° > 1°. The tertiary alcohols that are the initial oxidation products are not easily further oxidized. The geometry of the bicyclic rings (Bredt s rule) prevents both dehydration of the tertiary bridgehead alcohols and further oxidation to ketones. Therefore, oxidation that begins at a bridgehead position... 

On treatment with a base such as NaOMe or even LLAIH4, mono-cycloadducts of mesitonitrile oxide and polycyclic aromatic hydrocarbons have been cleaved to yield the corresponding oximes, which are oxidized to ketones by the Dess— Martin method. The same ketones have been obtained by reductive ring opening of the mono-cycloadducts with Raney Ni (438). 

Diols can be readily cleaved oxidatively to ketones by periodic acid (Eq. (17)). R2C—OH R2C—0x... 

Since tetranuclear platinum-blues are oxidized by 02 to Pt(III) dinuclear complexes and are reversively reduced to the platinum-blues and further to the Pt(II) dinuclear complexes, an attempt was made to use these complexes as catalysts for olefin oxidation to ketones and epoxides. The catalysts used were a-pyrrolidonato-bridged Pt-tan [Pt4(NH3)8(C4H6N0)4](N03)6 -2H20 (19), pivalamidato-bridged Pt-blue [Pt4(NH3)8(C5H10NO)4](NO3)5 (57), a-pyrrolidonato-tan [Pt4(NH3)8... 

The secondary alcohols are oxidized to ketones. In such oxidations, although air facilitates the process, but there is no oxygen uptake and since (CH3)2S has been isolated from the reaction products, it shows that DMSO is the oxidant. The mechanism in these oxidations is proabably as follows ... 

A very unusual Nazarov cyclization of propargyl vinyl ketones has been reported by Hashmi et al. (Eq. 13.16) [18]. Propargyl alcohol 50 was oxidized to ketone 51 with the Dess-Martin periodinane. Attempts to purify 51 by column chromatography on silica gel led to cyclopentenone 53 in 59% isolated yield. This suggests that the solid support catalyzed the isomerization of 51 to allenyl vinyl ketone 52, which was not isolated, but which underwent spontaneous cyclization to 53. This result is consistent with earlier observations of the great ease with which allenyl vinyl ketones undergo the Nazarov reaction (cf. 8, Eq. 13.2). 

Catalysed oxidation of non-activated haloalkanes by hypochlorite provides an attractive low-cost and convenient procedure for their conversion into carbonyl compounds [6] primary haloalkanes produce carboxylic acids and secondary haloalkanes are converted into ketones (Table 10.12). Secondary amines are oxidized to ketones under analogous conditions, whereas primary amines yield nitriles (Table 10.13) [1,2], o-Nitroanilines are oxidized to benzofurazan-1-oxides [15]. 

By indirect oxidation with electrogenerated NO3 radicals in f-butanol/ water/HN03/02, saturated hydrocarbons were oxidized to ketones with a statistical H-abstraction at the methylene... 

Benzyl alcohols Aryl alkyl carbinols (11) can be oxidized to ketones (12) by the direct electrochemical method (Eq. 4) since they possess their oxidation potentials at around 2.0 V versus SCE (saturated calomel electrode) however, cleavage products decrease the selectivity [14]. 

Secondary alcohols are oxidized to ketones and primary alcohols are oxidized to esters, when iodonium ion is used as a catalytic mediator as shown in Fig. 4 [35]. This method may have high potentiality in organic synthesis, since it requires only a catalytic amount of KI, whereas most of the hitherto known oxidations usually require more than one equivalent of the oxidizing agent. 

You learned earlier that primary alcohols are oxidized to aldehydes, and secondary alcohols are oxidized to ketones. You can think of the reduction of aldehydes and ketones as the reverse of these reactions. Aldehydes can be reduced to produce primary alcohols. Ketones can be reduced to produce secondary alcohols. 

Sauers and coworkers have applied the Paterno-Biichi reaction to engeneral formula 427 (Scheme XXXIV) Reductive cleavage of these products with lithium aluminium hydride is also regioselective and leads, following oxidation, to ketones... 

TABLE 30. Comparison of the results of metal-catalyzed alcohol oxidation to ketones, carboxylic acids or aldehydes using H2O2 or TBHP... 

The secondary alcohol groups in PVA may be oxidized to ketones, and the primary alcohol groups in carbohydrates may be oxidized to carboxylic acids. Although these reactions do not reduce the degree of polymerization, they do increase the degree of water solubility of the polymers. 

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