a mild, efficient and fast method for the oxidation of alcohols and trimethylsilyl, tetrahydropyranyl and methoxymethyl ethers to their corresponding carbonyl compounds using cro3 in the presence of rice husk ash (rha) is reported. all reactions were performed at room temperature in high to excellent yields. a new, efficient and green catalyst, heterogeneous reaction conditions, easy work-up of...

a mild, efficient and fast method for the oxidation of alcohols and trimethylsilyl and tetrahydropyranyl ethers to their corresponding carbonyl compounds using cro3 in the presence of sulfonic acid functionalized ordered nanoporous na+-montmorillonite (sanm) and under solvent-free conditions is reported. all reactions were performed at room temperature in high to excellent yields. ease of the p...

Alcohols, trimethylsilyl ethers and thiols were efficiently converted to their corresponding carbonyl and disulfides compounds using o-xylylenebis (triphenylphosphonium) dibromochromate (XTPPDBC). This reagent can selectively oxidize thiols to disulfides in the presence of alcohols and trimethylsilyl ethers in acetonitrile at room temperature.

The parameters affecting the separation and quantification of trimethylsilyl ethers of mono- and diglycerides have been investigated by gas-liquid chromatography with QF-1 and SE-30 as stationary phases and a flame ionization detector. Results have been compared with those obtained earlier for triglycerides. The isothermal characteristics of a range of trimethylsilyl ethers of mono- and diglyce...

The trimethylsilyl ethers of alditols with 3, 4, 5 and 6 carbon atoms were investigated. The mass spectra are unusually clearly correlated with the structures. The predominant fragmentations are cleavages in the carbon chain and rearrangement loss of trimethylsilanol. The spectra are closely related to those of the methyl ethers. A spectrum unambiguously identifies a compound as an alditol and ...

substituted naphthofurans and naphthopyrans were constructed at high temperature from allyl or propargyl naphthyl ethers via claisen rearrangement in moderate to good yields. also, substituted (trimethylsilyl)-naphthofurans were synthesized from the corresponding naphtofurans.

structurally different trimethyl silyl ethers are oxidized with bu4/nio4 in the presence of alcl3 and bf3 as catalysts in ch3cn and chcl3 under reflux conditions. the corresponding carbonyl compounds are isolated in good yields.

1,1’-(Ethane-1,2-diyl)dipyridinium bistribromide (EDPBT) was used as a chemoselective and effective organocatalyst for the silylation of hydroxyl groups as well as desilylation of trimethylsilyl ethers under mild conditions at room temperature with good to excellent yields.

An efficient and chemoselective cleavage of silyl ethers (primary, secondary and aromatic) by using catalytic quantities of trimethylsilyl bromide (TMSBr) in methanol is reported. A wide range of alkyl silyl ethers such as TBS, TIPS, and TBDPS can be chemoselectively cleaved in high yield in the presence of aryl silyl ethers. The deprotection of silyl esters was also achieved employing catalyti...

Substituted naphthofurans and naphthopyrans were constructed at high temperature from allyl or propargyl naphthyl ethers via Claisen rearrangement in moderate to good yields. Also, substituted (trimethylsilyl)-naphthofurans were synthesized from the corresponding naphtofurans.