T-Alkylation

Synthesis This route has been carried out successfully (Rec. Trav. Chem., 1958, 77, 854). Note that no AICI3 is needed for Friedel-Crafts alkylation with easily formed t-alkyl compounds. 

In the diaziridinimine field there is no sharp contrast between stable t-alkyl and unstable primary alkyl compounds. Both types are known as stable compounds (80H(14)1677). 

S)-tributyl[t-alkyl-3-(methoxymethoxy)-2-propenyl stannane yield 80% 90-95% ee... 

Aldehydes, 43 a-Chiral, 112 a/MJnsaturated, 85,110 /3-Aldchydosi lanes, 22 Aldol reaction, directed, 139 Alkoxytrimethylsilanes, 122 Alkyl lithium. 67 Alkyl silyl ethers, 91-97,127 Alkylation, 33 of ethyl glycinate, 88-89 t-Alkylation, 111-135... 

PhentEimine (11),used in the treatment of obesity, is a t-alkyl amine. The Ritter reaction, using HCN as the nitrile (p T63), is ideal for this,... 

The stability of nitroxides will be well known to readers acquainted with the spin-labelling technique (Berliner, 1976), but it must be recognized that nitroxides employed as spin labels or spin probes are almost invariably di-t-alkyl nitroxides. Diaryl and many aryl t-alkyl nitroxides are also sufficiently persistent to be isolated, and it has recently been shown that several acyl t-alkyl nitroxides can also be obtained pure (Perkins and Ward, 1973 Alewood et al., 1978). However, other nitroxides are less persistent. Monosubstituted nitroxides, RN(H)Q-, rapidly disproportionate to nitroso-... 

In the spin-trapping context, diaryl or aryl t-alkyl nitroxides are effectively stable. Both, however, when present in very high concentrations, may decay slowly by a bimolecular process (10), provided that steric constraints do not twist the aryl group out of conjugation with the nitroxide function. In contrast,... 

The tri-t-butylnitrosobenzene, TNB, is monomeric even in the solid state, but the principal advantage of this scavenger, exemplified in the mechanistic studies described in Section 3 (p. 47), is that it functions as an ambident spin trap (Terabe and Konaka, 1973). Thus, primary alkyl radicals add to form nitroxides in the normal way, but with t-alkyl radicals, addition occurs at oxygen, alkoxyaminyl radicals (ArNOR) being formed. Secondary alkyl radicals give mixtures of both species (Fig. 5). The alkoxyaminyl radicals have a lower g-value than the nitroxides (ca. 2.004 vs. 2.006) and their spectra are therefore centred at slightly higher field positions than those of the nitroxides. 

Hindered di-t-alkylamines RNHBu1 (R = t-Bu, t-octyl or 1-adamantyl) have been synthesized from t-alkylamines as follows. Reaction with peracetic acid gave the nitrosoalkanes RNO, which were treated with t-butyl radicals, generated from t-butylhydrazine and lead(IV) oxide, to yield t-butyloxyhydroxylamines. Reduction with sodium naphthalide in THF gave the products (equation 12). The di-t-alkyl-amines are inert to methyl iodide and dimethyl sulphate but can be alkylated by methyl fluorosulphonate42. 

Acylation reactions can also be greatly improved in this way, with t-alkyl- or sec-alkyl-manganese reagents reacting with acid chlorides in excellent yields [123]. The related addition-elimination to 3-ethoxy-2-cyclohexenone is also improved, resulting after acidic aqueous workup in 3-methyl-2-cyclohexenone [125]. The perilla-ketone 126 was prepared in an improved yield using copper(I) catalysis (Scheme 2.58) [129]. 

It is natural to presuppose that the reduction of nitro compounds should lead to the nitroso compounds, at least as an intermediate stage. Until quite recently, no reductive processes for the formation of nitrosoalkanes were known [3], More recently, some indirect evidence is said to show that, on electrolytic reduction of tertiary aliphatic nitro compounds, the final t-alkyl-hydroxylamines are produced by the intermediate formation of nitroso compounds which were not isolated [99]. 

For related reasons, and because their excited-state energies are lower than for dialkyl ketones, diaryl ketones and simple alkyl aryl ketones do not fragment on irradiation in solution, even at higher temperatures. This leads to a photostability that is one factor contributing to the successful employment of ketones such as benzophe-none tPh-CO) or acetophenone (PhCOMe) as triplet sensitizers. a-Cleavage for ketones in solution at room temperature is promoted if structural factors cause the bond adjacent to the carbonyl group to be somewhat weaker than normal. Hence t-alkyl ketones give decar-borylation products readily (4.5), as do benzyl ketones (4.6 and benzoin derivatives (4.7). 

The biradical intermediates have in some cases been detected by flash spectroscopy, or trapped by added reagents such as a t-alkyl nitroso compound. The enol produced by cleavage of the biradical is relatively inert at low temperatures, and it can be studied spectroscopically after irradiation of the ketone in solutions cooled below —50°C. There have been many mechanistic studies of the Norrish... 

Ito and co-workers have also used the Pd(OAc)2/t-alkyl isocyanide catalyst to affect the double silylation of carbon-carbon multiple bonds in an intramolecular system to yield silacarbocycles.59 Alkenes or alkynes that are tethered to a disilanyl group through a carbon chain, an ether linkage, or an amine functionality undergo intramolecular addition of the disilane moiety to the multiple bond. Activation of the disilane by the presence of electron-withdrawing groups on silicon is not necessary for the reaction to... 

Under copper(l) catalysis, excellent yields of dithioesters were obtained at -50°C, and t-alkyl magnesium halides, which led mainly to polymeric products without catalysis, gave yields above 90% in the presence of a catalytic amount (5-10 mol%) of copper(i) bromide [148]. 

RMgX (R= T, T alkyl allyl benzyl aryl vinylic alkynyl) MeO alkyl TL 31 4723 (1990)... 

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