Add to ORKGInternational audienceA simple and practical procedure for the reduction of acetals to ethers is described. It is based on the use of a 1,1,3,3-tetramethyldisiloxane (TMDS)–Pd/C system in the presence of a Brønsted acid as the co-catalyst. The reaction occurs under mild conditions and ethers are obtained in high yields
The TMS triflate catalyzed allylation of acetals to yield homoallyl ethers proceeds smoothly at room...
The allylation of acetals using allyltrimethylsilane is efficiently catalyzed by bismuth triflate (1...
1,2,2,6,6-pentamethylpiperidine (PMP) is shown to be an effective reducing agent for the radical cha...
We report an efficient two step process for the reduction of non-aromatic esters to the correspondin...
The development of methods to easily synthesize chemical structures is of great importance in the fi...
International audienceA protocol is described for the reduction of carboxylic acids to primary alcoh...
International audienceA simple and convenient method for the chemoselective reduction of nitriles in...
International audienceA protocol is described for the reductive cleavage of the C–O bond of aromatic...
The formation of acetals and ketals from aldehydes and ketones represents one of the most fundamenta...
International audience(Equation Presented) A simple procedure for the cleavage of triethylsilyl (TES...
International audienceThe palladium-catalysed reductive cleavage of methyl glucoside acetals has bee...
In the presence of {[K.18-Crown-6]Br3}n, a unique tribromide reagent, trimethylsilyl (TMS) ethers, t...
[[abstract]]A series of tetrahydropyranyl ethers are hydrolyzed to the corresponding alcohols in a C...
Aldehydes and ketones undergo a smooth reductive etherification by polymethylhydrosiloxane (PMHS) in...
The TMS triflate catalyzed allylation of acetals to yield homoallyl ethers proceeds smoothly at room...
The allylation of acetals using allyltrimethylsilane is efficiently catalyzed by bismuth triflate (1...
1,2,2,6,6-pentamethylpiperidine (PMP) is shown to be an effective reducing agent for the radical cha...
We report an efficient two step process for the reduction of non-aromatic esters to the correspondin...
The development of methods to easily synthesize chemical structures is of great importance in the fi...
International audienceA protocol is described for the reduction of carboxylic acids to primary alcoh...
International audienceA simple and convenient method for the chemoselective reduction of nitriles in...
International audienceA protocol is described for the reductive cleavage of the C–O bond of aromatic...
The formation of acetals and ketals from aldehydes and ketones represents one of the most fundamenta...
International audience(Equation Presented) A simple procedure for the cleavage of triethylsilyl (TES...
International audienceThe palladium-catalysed reductive cleavage of methyl glucoside acetals has bee...
In the presence of {[K.18-Crown-6]Br3}n, a unique tribromide reagent, trimethylsilyl (TMS) ethers, t...
[[abstract]]A series of tetrahydropyranyl ethers are hydrolyzed to the corresponding alcohols in a C...
Aldehydes and ketones undergo a smooth reductive etherification by polymethylhydrosiloxane (PMHS) in...
The TMS triflate catalyzed allylation of acetals to yield homoallyl ethers proceeds smoothly at room...
The allylation of acetals using allyltrimethylsilane is efficiently catalyzed by bismuth triflate (1...
1,2,2,6,6-pentamethylpiperidine (PMP) is shown to be an effective reducing agent for the radical cha...