Sulfonium salts synthesis

Sodium hydride dimethyl sulfoxide Ring closures with sulfoxonium and sulfonium salts Synthesis of oxido compounds from oxo compounds Cyclopropanes from ethylene derivatives... 

Poly(arylene vinylenes). The use of the soluble precursor route has been successful in the case of poly(arylene vinylenes), both those containing ben2enoid and heteroaromatic species as the aryl groups. The simplest member of this family is poly(p-phenylene vinylene) [26009-24-5] (PPV). High molecular weight PPV is prepared via a soluble precursor route (99—105). The method involves the synthesis of the bis-sulfonium salt from /)-dichloromethylbenzene, followed by a sodium hydroxide elimination polymerization reaction at 0°C to produce an aqueous solution of a polyelectrolyte precursor polymer (11). This polyelectrolyte is then processed into films, foams, and fibers, and converted to PPV thermally (eq. 8). 

When bromoacetyl chloride is used instead of bromoacetic acid, the anilide 33 is formed at the first stage. Its subsequent cyclization also leads to 32. This approach to benzotellurazinone is similar to that developed for the synthesis of 2//-l,4-benzothiazin-3(4//)-ones (66CJC1247). Significantly, attempts to isolate the intermediate sulfonium salts analogous to 30 were unsuccessful. 

Solladie-Cavallo has recently reported a two-step asymmetric synthesis of dis-ubstituted N-tosylaziridines from (R,R,R,Ss)-(-)-sulfonium salt 2 (derived from Eliel s oxathiane see Section 1.2.1.1) and N-tosyl imines with use of phosphazine base (EtP2) to generate the ylide (Scheme 1.42) [67], Although the diastereoselectiv-ity was highly substrate-dependent, the enantioselectivities obtained were very high (98.7-99.9%). The chiral auxiliary, although used in stoichiometric quantities, could be isolated and reused, but the practicality and scope of this procedure is limited by the use of the strong - as well as expensive and sensitive - phospha-zene base. 

It is well known that aziridination with allylic ylides is difficult, due to the low reactivity of imines - relative to carbonyl compounds - towards ylide attack, although imines do react with highly reactive sulfur ylides such as Me2S+-CH2-. Dai and coworkers found aziridination with allylic ylides to be possible when the activated imines 22 were treated with allylic sulfonium salts 23 under phase-transfer conditions (Scheme 2.8) [15]. Although the stereoselectivities of the reaction were low, this was the first example of efficient preparation of vinylaziridines by an ylide route. Similar results were obtained with use of arsonium or telluronium salts [16]. The stereoselectivity of aziridination was improved by use of imines activated by a phosphinoyl group [17]. The same group also reported a catalytic sulfonium ylide-mediated aziridination to produce (2-phenylvinyl)aziridines, by treatment of arylsulfonylimines with cinnamyl bromide in the presence of solid K2C03 and catalytic dimethyl sulfide in MeCN [18]. Recently, the synthesis of 3-alkyl-2-vinyl-aziridines by extension of Dai s work was reported [19]. 

An alternative process for the synthesis of vinylepoxides was clearly needed, so reactions with stoichiometric amounts of chiral sulfide were investigated (Scheme 9.16a) [74]. Indeed, when benzyl sulfonium salt 20 was treated with unsaturated aldehydes, the ees and des were high in all cases, whereas the yields [75] were highly substrate-dependent. The same products could be formed by treatment of an unsaturated sulfonium salt with benzaldehyde, but the yields and se-lectivities were generally slightly lower. 

Sulfur ylides have several applications as reagents in synthesis.282 Dimethylsul-fonium methylide and dimethylsulfoxonium methylide are particularly useful.283 These sulfur ylides are prepared by deprotonation of the corresponding sulfonium salts, both of which are commercially available. 

The synthesis of a bridgehead sulfonium salt analogue 59, of the naturally occurring glycosidase inhibitor castanospermine, proceeded by a multistep procedure starting from 5-thio-d-glucopyranose pentaacetate <2000JA10769>. The desired bicyclic sulfonium salt 57 could not be obtained from the key bromide precursor... 

Sulfur ylides are a classic reagent for the conversion of carbonyl compounds to epoxides. Chiral camphor-derived sulfur ylides have been used in the enantioselective synthesis of epoxy-amides <06JA2105>. Reaction of sulfonium salt 12 with an aldehyde and base provides the epoxide 13 in generally excellent yields. While the yield of the reaction was quite good across a variety of R groups, the enantioselectivity was variable. For example benzaldehyde provides 13 (R = Ph) in 97% ee while isobutyraldehyde provides 13 (R = i-Pr) with only 10% ee. These epoxy amides could be converted to a number of epoxide-opened... 

One procedure for the synthesis of these title ring systems appeared recently <2003S1079>. Yadav and Kapoor described that the transformation of some oxadiazole and thiadiazole derivatives bearing specially substituted methylsulfinyl side chain 131, when reacted with thionyl chloride, give ring-closed compounds 134. The reaction was carried out in pyridine under reflux conditions in 74-79% yield. As shown in Scheme 25, the authors assume that the first step is the formation of the sulfonium salt 132 which undergoes cyclization with hydrogen chloride and sulfur dioxide elimination to 133 and, finally, demethylation of this intermediate leads to the final product 134. 

The utility of sulfur ylides in organic synthesis demands methods for the efficient preparation of the precursor sulfonium salts.2 Among the... 

From the synthetic viewpoint the optical resolution of sulfonium salt 110 is of great interest because its enantiomers served as starting material for the synthesis of chiral a-dehydrobiotin 111(156). 

It is interesting to note that asymmetric synthesis of the sulfonium salt 112 was recently reported by Kobayashi (157). He found that... 

In addition to routes involving resolution and asymmetric synthesis, optically active sulfonium salts have been prepared in a stereospecific way by Andersen (158,159). Thus, synthesis of the optically active dialkyl-p-tolylsulfonium salts 114 from the optically active ethoxy-sulfonium salt 115 was accomplished by the addition of alkyl Grig-nard or dialkylcadmium reagents. This reaction occurs with inversion... 

In their important work on the synthesis and properties of optically active chlorosulfurane (+)-177, Martin and Balthazor (195) deduced its absolute configuration by means of chemical correlations. Reaction of (+)-l 77 with silver tetrafluoroborate yields cyclic sulfonium salt 198, which was hydrolyzed without isolation under alkaline conditions to give sulfoxide (-)-(5 -180, from which (+)-177 was obtained. Assuming that the conversion (+)-l 77 -> 198 proceeds with... 

The basic poly(phenylene vinylene) (PPV) polymer is commonly prepared by the sufonium prepolymer route developed by WessUng and Zimmerman in 1968 but much modified by subsequent workers. The synthesis starts from 1,4-bis(chloromethyl)benzene, via the bis-sulfonium salt formed by reaction with tetrahydrothiophene, and then polymerisation is effected to give the prepolymer by reaction with lithium hydroxide (Figure 3.39). Because of the inherent insolubility of PPV it is this prepolymer that is used to form the film coating on the substrate, for example by using a doctor blade technique. The prepolymer is converted into PPV on the substrate by heating in an oven under vacuum at 200 °C for 8-10 h. 

Sulfonium salts have been prepared on insoluble supports by S-alkylation of thioethers (Figure 8.2) only as synthetic intermediates. These compounds can be used to alkylate carboxylates [168] and halides [65], or as electrophiles for the Suzuki cross-coupling reaction (see Entry 7, Table 3.48 [169]). Sulfonium salts are also C,H-acidic, and can be used as intermediates for the synthesis of epoxides (Entry 7, Table 15.1 [170]). 

Synthesis of epoxides from carbonyl compounds and sulfonium salts... 

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