Sulphones allylic

Subsequently, Julia, Uguen and Callipolitis104 105 used both lithium metal in ethyl-amine and sodium amalgam in ethanol to effect reductive cleavages of j8-hydroxysulphones or of allylic sulphones. The latter reaction is part of a synthetic sequence for the construction of alkenes that has been used with some considerable success... 

Benzylic, allylic and propargylic positions enhance the cathodic cleavage rate of C— heteroatom bonds as, for example, in the reduction of benzylic and allylic halides or alcohols56. Similar activated sulphones, due to their acidity, are in a class apart. Figure 8 shows the similitude between the cathodic behaviour of an allylic sulphone and its isomer, i.e., the corresponding vinylic sulphone when the electrolyses are run in an aprotic solvent. However, in the presence of an excess of proton donor, discrepancies appear. 

However, a very unexpected situation is found24 for the phenyl allyl sulphone (53), for which a one-electron cleavage occurs in aprotic non-aqueous solvents. The allyl radical is apparently not electroactive at the cleavage potential, and forms the dimer. Therefore, in this one-electron bond scission no strong base is formed and the isomerization into the vinylic isomer is not observed (Figure 9). Similarly, the cleavage of phenyl propargyl... 

FIGURE 10. Voltammetric curves of fully aliphatic allylic sulphones (c = 3 x 10-3 M) in DMF/TBAP 0.1 m electrolyte, stationary mercury electrode, sweep rate 10 mV s—1 (a) and (b) curves in aprotic DMF (c) response of the sulphone, (b) with phenol 10-2 m (after Reference 26). 

It has been found50 that such a multielectron step does not exist with 58, which exhibits a classical two-electron scission. In general, allylic sulphones (59) without an unsaturated system in a suitable position are not reducible. Thus, they do not exhibit a cathodic step in protic solutions. However, in aprotic media the isomerization may be base catalyzed, since small amounts of electrogenerated bases from electroactive impurities, even at low concentration, may contribute to start the isomerization. Figure 10 shows the behaviour of t-butyl allylic sulphone which is readily transformed in the absence of proton donor. On the other hand, 60 is not isomerized but exhibits a specific step (Figure 10, curve a) at very negative potentials. 

Sulphones (coni.) allenic - see Allenic sulphones allyl - see Allyl sulphones aryl unsaturated alkyl - see Aryl unsaturated alkyl sulphones aryl vinyl - see Aryl vinyl sulphones as radiolytic products 907 bicyclic - see Bicyclic sulphones bis(/ -hydroxyalkyl) - see Bis... 

Allyl sulphones can be converted to dienes by alkylation and elimination of sulphinic acid under basic conditions (equation 64)105. Several vitamin A related polyenes have been synthesized following this two-step protocol (Table 10)106. The poor leaving-group ability of the arylsulphonyl group requires treatment with strong base for elimination. However, elimination of the allylsulphonyl group takes place readily under palladium catalysis (equation 65)107. Vinyl sulphones can be converted to dienes via Michael addition, alkylation with allyl halides and elimination of sulphinic acid sequence (equation 66)108. 

TABLE 10. Synthesis of vitamin A and related compounds through allyl sulphones... 

As an alternative to radical chlorination, use has been made of carbon tetrachloride and hexachloroethane in the presence of a quaternary ammonium salt, as source of the chloronium ion for reaction with activated alkylbenzenes [38], Benzyl chlorides need the additional activation of a nitro group for their conversion into the corresponding nitrobenzotrichlorides, whereas benzal chlorides do not need the extra activation for a similar conversion. The same synthetic protocol, using hexachloroethane, has been used for the conversion of allylic sulphones into the 1,1-dichloro derivatives [39],... 

The reaction of methylenesulphones with allyl halides in the presence of quaternary ammonium salts produces the 1-allyl derivatives [52], unlike the corresponding reaction in the absence of the catalyst in which the SN- product is formed (Scheme 6.5). In contrast, alkylation of resonance stabilized anions derived from allyl sulphones produces complex mixtures [51] (Scheme 6.6). Encumbered allyl sulphones (e.g. 2-methylprop-2-enyl sulphones) tend to give the normal monoalkyl-ated products. Methylene groups, which are activated by two benzenesulphonyl substituents, are readily monoalkylated hydride reduction leads to the dithioacetal and subsequent hydrolysis affords the aldehyde [61]. 

As reactions 68 and 69 above exemplify, the substitution of the allylsilane usually takes place with an allylic shift (Se2 ). This can be synthetically useful, for example in the isomerization of allyl sulphones 123 to vinyl sulphones 124 (equation 74)145. The reaction is also highly stereospecific (>90% E) (vide infra). 

Trost has disclosed some new chemistry of allylic sulphones which... 

Isomerizations and Rearrangements An optically active allylic sulphone has been generated via a... 

There has been considerable activity surrounding alkenyl sulphones this year. The 1- and 2- arylsulphonyl alkenes (274) and (275) have been obtained by either the sulphonylmercuration or iodosulphisation of 1-alkenes. If allylic protons are present, isomerisation to give allylic sulphones is facile. a-Substituted sulphones 77).270... 

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