Ketones are reported to be conveniently converted into their α-tolylsulfinylated derivatives. This new procedure is based on the reaction of their corresponding trimethylsilyl enol ethers with p-toluenesulfinyl p-tolylsulfone in the presence of tris(dimethylamino)sulfur trimethylsilyldifluoride (TAS-F). Considering that β-ketosulfoxides are key intermediates for the preparation of α,β-unsaturated ketones, this procedure turns out to be of rather broad synthetic relevance
A direct Csp3–H bond oxidative thioesterification of methyl ketones with aromatic thiols/disulfides ...
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethyls...
The development of new synthetic methods in organic chemistry is of importance because new routes to...
Ketones are reported to be conveniently converted into their α-tolylsulfinylated derivatives. This n...
<div><p>α-Acyloxy aldehydes, as O-protected α-hydroxy aldehydes, have been prepared in good yields v...
Treatment of TIPS enol ethers with PhIO/TMSN3 followed by desilylation/elimination with fluoride ion...
Abstractz Ultrasound enhvlces substul~$lly the rites of a-tosyloxyl;ltion of ketones with [hydmxy(to...
<div><p></p><p>With 1,1,1-trifluoro-2-iodoethane as catalyst, a novel and efficient procedure has be...
Ketones and carboxylic acid esters are conveniently converted to their α-sulfenylated derivatives. T...
A practical method for the synthesis of 3-deoxy-l-ketohexoses is described. Both d- and l-ketohexose...
Silyl enol ethers can be effectively alkylated with primary n-alkyl iodides in the presence of silve...
Silyl enol ethers (2) react with tributyl [(phenylthio) chloromethyl] stannane (1) in the presence o...
Stereoselective 9-step conversions of the ketone 17 into the tricyclic ketone 31 via two similar syn...
Contains fulltext : 19347_silyanoxs.pdf (publisher's version ) (Open Access)In thi...
alpha-Ketosulphides of benzothiazole 1 react with allylic carbonates in the presence of palladium a...
A direct Csp3–H bond oxidative thioesterification of methyl ketones with aromatic thiols/disulfides ...
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethyls...
The development of new synthetic methods in organic chemistry is of importance because new routes to...
Ketones are reported to be conveniently converted into their α-tolylsulfinylated derivatives. This n...
<div><p>α-Acyloxy aldehydes, as O-protected α-hydroxy aldehydes, have been prepared in good yields v...
Treatment of TIPS enol ethers with PhIO/TMSN3 followed by desilylation/elimination with fluoride ion...
Abstractz Ultrasound enhvlces substul~$lly the rites of a-tosyloxyl;ltion of ketones with [hydmxy(to...
<div><p></p><p>With 1,1,1-trifluoro-2-iodoethane as catalyst, a novel and efficient procedure has be...
Ketones and carboxylic acid esters are conveniently converted to their α-sulfenylated derivatives. T...
A practical method for the synthesis of 3-deoxy-l-ketohexoses is described. Both d- and l-ketohexose...
Silyl enol ethers can be effectively alkylated with primary n-alkyl iodides in the presence of silve...
Silyl enol ethers (2) react with tributyl [(phenylthio) chloromethyl] stannane (1) in the presence o...
Stereoselective 9-step conversions of the ketone 17 into the tricyclic ketone 31 via two similar syn...
Contains fulltext : 19347_silyanoxs.pdf (publisher's version ) (Open Access)In thi...
alpha-Ketosulphides of benzothiazole 1 react with allylic carbonates in the presence of palladium a...
A direct Csp3–H bond oxidative thioesterification of methyl ketones with aromatic thiols/disulfides ...
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethyls...
The development of new synthetic methods in organic chemistry is of importance because new routes to...