an efficient and selective method for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds under solvent-free conditions
Authors
abstract
o-xylylenebis (triphenylphosphonium peroxymonosulfate) (1) was easily prepared from an aqueous solution of oxone and o-xylylenebis- (triphenylphosphonium bromide). this compound (1) is a useful and selective reagent for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds. the reaction was carried out under solvent-free conditions and in the presence of catalytic amount of aluminium chloride. this method shows a good selectivity in oxidation of oximes, semicarbazones and phenylhydrazones in the presence of aliphatic and aromatic alcohols. the advantages of the present method include good functional group tolerance, high yields of products, simple experimental procedure and purification, no solvent and short reaction times.
similar resources
An efficient and selective method for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds under solvent-free conditions
o-Xylylenebis (triphenylphosphonium peroxymonosulfate) (1) was easily prepared from an aqueous solution of oxone and o-xylylenebis- (triphenylphosphonium bromide). This Compound (1) is a useful and selective reagent for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds. The reaction was carried out under solvent-free conditions and in the presence...
full textAn efficient and selective method for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds under solvent-free conditions
o-Xylylenebis (triphenylphosphonium peroxymonosulfate) (1) was easily prepared from an aqueous solution of oxone and o-xylylenebis- (triphenylphosphonium bromide). This Compound (1) is a useful and selective reagent for conversion of oximes, semicarbazones and phenylhydrazones to the corresponding carbonyl compounds. The reaction was carried out under solvent-free conditions and in the presence...
full textEfficient Synthesis and Deprotection of Semicarbazones under Solvent-Free Conditions
Effective methodologies for efficient preparation of semicarbazones from aldehydes or ketones via milling and the subsequent regeneration of the parent carbonyls by gaseous nitrogen dioxide are described under solid-solid and gas-solid reaction conditions, respectively. These methods are fast, simple and environmentally benign which do not require the use of any auxiliaries such as catalyst...
full textefficient synthesis and deprotection of semicarbazones under solvent-free conditions
effective methodologies for efficient preparation of semicarbazones from aldehydes or ketones via milling and the subsequent regeneration of the parent carbonyls by gaseous nitrogen dioxide are described under solid-solid and gas-solid reaction conditions, respectively. these methods are fast, simple and environmentally benign which do not require the use of any auxiliaries such as catalysts or...
full textA Fast and Efficient Method for the Synthesis of 1,5-Benzodiazepine Derivatives Under Solvent-Free Conditions
Silica sulfuric acid is found to catalyze efficiently the condensation of o-phenylenediamines with various linear and cyclic ketones to afford the corresponding 1,5-benzodiazepines in quantitative yields under solvent-free conditions at room temperature
full textSelective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with N-chlorosaccharin under mild and solvent-free conditions
An efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of N-chlorosaccharin (1 mol %) and 3, 4-dihydro-2H-pyran under solvent-free condition at room temperature. Benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, ...
full textMy Resources
Save resource for easier access later
Journal title:
iranian journal of catalysisPublisher: islamic azad university, shahreza branch
ISSN 2252-0236
volume 5
issue 4 2015
Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023