Sulphenates reactions

Jones and coworkers200 found that a variety of sulphenic acids may be generated by thermolysis of the readily available /J-cyanosulphoxides (equation 81) and observed their highly regiospecific addition also to non-conjugated alkynes (Table 12). As expected for a pericyclic mechanism, the reaction afforded the product of a stereospecific cis-addition. However, the regioselectivity of the addition suggests that the partial carbon-sulphur bond in the transition state 148 is polarized in such a way that the carbon atom has some cationic character (equation 82). 

The allyl sulphenate-allyl sulphoxide rearrangement is a general reaction and is applicable to structurally diverse allyl alcohols204,205 (Table 13). Mechanistically, it represents a typical example of a [2,3]-sigmatropic rearrangement as shown by the detailed investigations of Mislow and Braverman and their coworkers. 

Reaction of alkynols 156 with benzenesulphenyl chloride afforded either the vinylacety-lene sulphoxides 157 or the allene sulphoxides 158 depending upon the substitution pattern of alkynols 156. Vinylacetylene sulphoxides 157 result from a [2,3]-allylic rearrangement of the sulphenate ester 159 (equation 88). In the case of the cyclic... 

For a recent discussion on the stereochemical aspects of the Diels-Alder reaction with vinyl sulphoxides see References 662, 663. It should be pointed out that vinyl sulphoxides can be considered in [2 + 4]-cycloadditions as acetylene synthons since the sulphinyl moiety may be removed from the product by sulphenic acid elimination. Paquette and coworkers took advantage of this fact in the synthesis of properly substituted anthracenes 562664, (equation 360). 

Sulphonyl phosphates, reactions of 638 Sulphonyl radicals 215 cyclization of 1099 ESR spectra of 1090-1093 formation of 1094-1098 structure of 1090-1094 thermodynamic data for 1094 Sulphonyl sulphenes 196 Sulphonyl sulphoxides alkylation of 311 synthesis of 262... 

Rearrangement of acetylenic sulphenates to the allenic sulphoxides 151 was discovered when the synthesis of propargylic ester of trichloromethanesulphenic acid 152 was attempted (equation 86). This reaction is of general scope and gives very good yields of allenic sulphoxides (Table 14) from structurally diverse cohols and various sulphenyl chlorides Reaction of alkynols 153 with benzenesulphenyl chloride in the presence... 

Reaction of the carbanion of chloromethyl phenyl sulphoxide 409 with carbonyl compounds yields the corresponding 0-hydroxy adducts 410 in 68-79% yield. Each of these compounds appears to be a single isomer (equation 242). Treatment of adducts 410 with dilute potassium hydroxide in methanol at room temperature gives the epoxy sulphoxides 411 (equation 243). The ease of this intramolecular displacement of chloride ion contrasts with a great difficulty in displacing chloride ion from chloromethyl phenyl sulphoxide by external nucleophiles . When chloromethyl methyl sulphoxide 412 is reacted with unsymmetrical ketones in the presence of potassium tcrt-butoxide in tert-butanol oxiranes are directly formed as a mixture of diastereoisomers (equation 244). a-Sulphinyl epoxides 413 rearrange to a-sulphinyl aldehydes 414 or ketones, which can be transformed by elimination of sulphenic acid into a, 8-unsaturated aldehydes or ketones (equation 245). The lithium salts (410a) of a-chloro-/ -hydroxyalkyl... 

Sulphoxides and selenoxides undergo syn elimination under thermal conditions. A 1,4-elimination of sulphenic acid from an allyl sulphoxide leads to dienes (equation 20)50. Precursor sulphoxides are generated by oxidation of corresponding sulphides. This reaction, however, did not give good results when applied to more complicated systems51. 

S-chloro-phosphinothiolates with phosphorus trichloride leads to desulphurization.65 The reaction of sulphenates with phosphines leads to deoxygenation,66 and not (as previously reported) to desulphurization. Even when the ion pair (52 R1 = R2 = Me, R3 = Bun) was generated from the sulphide (53), the reaction still led to... 

The latter anomalous" behaviour has been ascribed to the direct formation of pentacoordinated products from P(III) and the substrate as distinct from nucleophilic displacement by phosphorus so that the stability of the T.S. leading to the pentacoordinated molecule dictates the rate. >11 >LI There is no doubt that several reactions which display the anomalous rate sequence (eg with peroxides, sulphenate esters and dithietenes) do give pentacoordinated products and the proposal is given further support by the reaction of diethyl peroxide with a series of cyclic phosphines in which the rate sequence parallels the stability of the P(V) products.II Furthermore, under the appropriate conditions pentacoordinated products are also formed from alkenes (eqn. 2) and alkynesl . (eqn. 3) and although rate data is only available for... 

Schenone and coworkers have shown in a large number of papers that tertiary aminomethyleneketones react as heterodienes, e.g. with sulphene generated from aliphatic sulphonyl chlorides and triethylamine as a heterodienophile, to yield / -aminosultons in a Diels-Alder reaction. An early simple example is reported by Opitz270 (equation 199). 

Sulphene or phenylsulphene adds to the enaminothiones 217 in a two-step reaction to yield 1,2-dithiin dioxides 317 (equation 130)118,158. 

Although the fragmentation reactions of the molecular ions of sul-phones and sulphoxides varied, the first step in rationalizing their behaviour was initial isomerization to sulphinate (64) and sulphenate esters (65). A variety of reactions of this type has been collated by Fields and Meyerson (1968), who pointed out that isomerization of sulphoxides to sulphenate esters was a known thermal reaction (see also, Kutz and Weininger, 1968, Kinstle et al., 1968b). In experiments designed to compare the mass-spectral and thermal behaviour of a series of sulphoxides, it was observed that the thermal isomerization appeared to proceed, but no comparable behaviour was observed in the mass spectra (Entwistle et al., 1967). 

Aminopenicillanic acid (8) was converted to 6(5)-bromopenicillanic acid by trapping of the diazo-intermediate with hydrogen bromide. Esterification of the dicyclohexylamine salt (93) with p-methoxybenzyl bromide, followed by oxidation, afforded the sulphoxide (94) in 60% yield from 6-APA. Elaboration of this sulphoxide to the disulphide (96) was effected by the procedure established by Kamiya et al. [98] the sulphenic acid (95), formed by heating the sulphoxide to reflux in toluene, was intercepted by reaction with 2-mercaptobenzothiazole to yield the disulphide (96). The latter was transformed by base-catalysed double bond isomerization to the conjugated ester disulphide (97) [95% yield from (94)]. Reductive formylation of disulphide (97) then provided the formylthio-derivative (98). Cyclization of the oxalimide (99), obtained by ozonolysis of... 

Other reagents which react with arsonium ylides are phenyl sulphine and phenyl sulphene (equation 19). Ethyl cinnamate is also a product of the latter reaction. 

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