Thioketones, oxidation

Hydrogen chloride has also been eliminated from sulfinyl chlorides by addition of triethylamine. The thioketone oxide obtained from 9-fluorene-sullinyl chloride reacted with morpholinocyclohexene to give a zwitterionic adduct (475). 

Thioaldehydes and thioketones oxidized at sulfur are additively named as thioaldehyde oxides, dioxides and thioketone oxides, dioxides, respectively. Besides, the traditional names sulfine and sulfene are still used for these species. 

Two further compounds are on the borderline of stability. The oxathiirane (14), obtained by photorearrangement of a thioketone 5-oxide, could be characterized by its UV spectrum (76JCS(P1)1404). Thiazirine (15) was stable only at 15 K (78JCS(P1)746). 

The cyclic thioketone, 3-oxotctrahydrothiophene (11), gives a mixture of enamines (12,13) when caused to react with a secondary amine such as piperidine or pyrrolidine (31). The enamine mixture can be reduced to the 3-aminotetrahydrothiophene using formic acid or oxidized to the 3-amino-thiophene using diisopentylsulfide. 

A ring opening of the dithiirane 39 to the thioketone 5-sulfide 35 was proposed for the reaction of thiobenzophenone 5-oxide (40) with the thioketone 41 (81LA187). Tlie conjugation with the phenyl group would stabilize 35 relative to the dithiirane form. 

Tlie isolable dithiiranes (4 and 7) are fairly stable under acidic conditions but quickly lose a sulfur atom to give the corresponding thioketones under basic conditions (97BCJ509). Tliey are quite sensitive toward amines and phosphines. Oxidation with MCPBA gave the corresponding dithiirane 1-oxides in high yields. 

Tlie thioketone 5-oxide 85, generated from allene 86 and SOCk in situ, decomposes to give the alkene 87. A mechanism, involving the transient formation of the 1,2-dithietane 88 (by dimerization of 85 followed by rearrangement), was proposed (85AGE855). 

All unexpected reaction is the formation of dithiete 175, thiirene 1-oxide 185, and thioketone 186 by the treatment of di-l-adamantylacetylene with S2CI2 (99UPl).Tlie yield of each compound is 30% at most. 

Thermolysis of 16e,f in either solution or gas phase (150-350 °C) gave deuteriated ethylenes (i.e. 40e from 16e and 41f from 16f) with about 95% retention of stereochemis-try ". Similarly, pyrolysis of the stereoisomeric 2,3-diphenylthiirane oxides 16g,h proceeded smoothly to yield stilbenes and sulfur monoxide in more than 70% yield . The extrusion of SO from the trans-isomer proceeds almost stereospecifically, while that from the cis-isomer occurs with complete loss of stereochemistry. This indicates the intervention of a stepwise mechanism, and not a symmetry-allowed nonlinear chelatropic reaction . Based on the fact that all attempts to trap the intermediate with 1,3-dipolarophiles were in vain, whereas a 1 1 adduct was obtained in good yield (about 60%) with the carbon radical scavenger di-p-anisyl thioketone, a mechanistic scheme as depicted in equation 10 has been proposed . Although the radical intermediates are capable of internal rotation about the carbon-carbon bond, for the 2,3-diphenyl case (i.e. 16g,h), the rotation would be... 

Diaryl thioketones are converted by diiron enneacarbonyl into products of orthometallation.141 Oxidative or photochemically induced deligation of these complexes provides an unusual and valuable synthetic entry into compounds in the uncommon isobenzothiophene category142,151 (Scheme 84). Moreover, the photochemical procedure provides the novel complex, (tetracyanoethylene)tetracarbonyl iron. The orthometallated complexes (68) can also be used to prepare isobenzofurans (see Section IV,B,5). 

Common synthesis of disulfonium dications involves formation of a S-S bond by oxidative coupling of two sulfide moieties. Involving for oxidative generation of S-S bond, thiocarbonyl compounds can lead to new-type dications containing disulfide moieties between two positively charged fragments. There are several disulfide dications of this type derived from thioureas, thiocarbon-ates and thioketones as well as selenium derivatives.137 148... 

N-benzyladamantyl-2-imines, and 2-methyleneadamantanes were studied (352, 353). In particular, X-ray single-crystal analysis confirmed the configuration of the oxathiazoline 185, resulting from the favored attack of nitrile oxide on the 5-fluoroadamantane-2-thione. 2-Silyl-substituted oxathiazole 186 was synthesized by the 1,3-dipolar cycloaddition reaction of phenyl triphenylsilyl thioketone with 4-chlorobenzonitrile oxide (354). 

Oxidation of tetrathioianes (8) with DMDO gave mixtures of dithiirane 1-oxides (10) and thioketones (11) (Scheme 5). The existence of the intermediate tetrathioiane 1-oxides (9) was verified by NMR of the cooled and evaporated reaction mixture. ... 

Like its monomeric counterpart, the polymeric reagent is inert to simple amines, amides, alcohols and phenols, but easily oxidizes thiols to disulphides, phosphines to phosphine oxides, hydroquinone and catechol to quinones, and thioketones, thioesters and trithiocar-bonates to the corresponding 0x0 derivatives, in dichloromethane, chloroform or acetic... 

Sulfur dioxide reacts with aliphatic thioketone (5)-methylides in a sealed tube at 100 °C and l,2,4-oxadithiolane-2-oxides (138) are obtained. None of the regioiso-meric cycloadduct was formed (177). 

Oxidation Carbon-Sulfur Systems. The most common metabolic process that affects a C-S system is S-oxidation. The S atom is oxidized to a sulfoxide. In the case of thioketones, the C=S double bond is converted to a C=0 bond. For thioethers, oxidative S-dealkylation is a possibility. 

Dithietanes, dimers of thioketones, are best stabilized by electron withdrawing groups on the ring. They are oxidized to bis-sulfoxide derivatives quite readily, and in at least one case the intermediate dioxide was isolated (Scheme 29) (80AG(E)203). 

Two types of reaction are observed for thioketones that do not have parallels in ketone photochemistry. The first is photocyclization in thioketones with polycyclic aromatic groups (4.104), where the sulfur atom forms a new bond to the aromatic system. The second is photo-oxidation by singlet oxygen to give the corresponding carbonyl compound 4.10S), possibly via a 1,2,3-dioxathietane formed as a result of initial cycloaddition. 

In the absence of air, benzene solutions of (6) are unusually stable. However, in the presence of oxygen photooxidation occurs readily to give a mixture of thioketone (150), diketone (151) and thioketone S- oxide (152). The formation of all these products can be rationalized on the basis of cycloaddition of oxygen across the 1,3-positions resulting in an unstable thioozonide (153), which collapses to the observed products (Scheme 44)... 

---