A new procedure for the protection of aldehydes and ketones as thioacetals promoted by catalytic amount of p-toluene-sulfonic acid and silica gel has been developed. This procedure offers versatility, short reaction time, excellent yield, good selectivity, and flexibility in terms of choice of solvent that can be utilized in this reaction. The procedure is easy to carry out and does not require aqueous work-up. A simple filtration followed by removal of solvent in most cases produces pure product. © Georg Thieme Verlag Stuttgart
A simple and efficient thiol-mediated addition of ketones to aromatic and aliphatic aldehydes is rep...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...
1291-1295Silica sulfuric acid has been found to be an efficient and reusable catalyst for chemosele...
<p></p> <p>Protection of <i>p</i>-anisaldehyde with 1,3-propanedithiol under UV irradiation without ...
We describe herein the use of glycerol as an efficient and a recyclable solvent in the thioacetaliza...
An important and surprising finding that the acetalization and ketalization of aldehydes and ketones...
Aldehydes and ketones can be protected as acetals and ketals by treatment with trimethyl orthoformat...
1,1-Diacetates are prepared in excellent yields from aldehydes and acetic anhydride under solvent-fr...
Aldehydes and ketones, when exposed to alkyl thiols or suitable alkane dithiols in presence of titan...
Thiosilanes react efficiently with simple aldehydes and ketones when catalyzed with ZnI_2 to produce...
Thioacetals derived from aldehydes and ketones can be unmasked to the corresponding carbonyl compoun...
Neat chlorosulfonic acid reacts with silica gel to give silica sulfuric acid in which sulfuric acid ...
<div><p>α-Acyloxy aldehydes, as O-protected α-hydroxy aldehydes, have been prepared in good yields v...
International audienceA range of carbonyl compounds including aliphatic and aromatic aldehydes and k...
A simple and efficient thiol-mediated addition of ketones to aromatic and aliphatic aldehydes is rep...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...
1291-1295Silica sulfuric acid has been found to be an efficient and reusable catalyst for chemosele...
<p></p> <p>Protection of <i>p</i>-anisaldehyde with 1,3-propanedithiol under UV irradiation without ...
We describe herein the use of glycerol as an efficient and a recyclable solvent in the thioacetaliza...
An important and surprising finding that the acetalization and ketalization of aldehydes and ketones...
Aldehydes and ketones can be protected as acetals and ketals by treatment with trimethyl orthoformat...
1,1-Diacetates are prepared in excellent yields from aldehydes and acetic anhydride under solvent-fr...
Aldehydes and ketones, when exposed to alkyl thiols or suitable alkane dithiols in presence of titan...
Thiosilanes react efficiently with simple aldehydes and ketones when catalyzed with ZnI_2 to produce...
Thioacetals derived from aldehydes and ketones can be unmasked to the corresponding carbonyl compoun...
Neat chlorosulfonic acid reacts with silica gel to give silica sulfuric acid in which sulfuric acid ...
<div><p>α-Acyloxy aldehydes, as O-protected α-hydroxy aldehydes, have been prepared in good yields v...
International audienceA range of carbonyl compounds including aliphatic and aromatic aldehydes and k...
A simple and efficient thiol-mediated addition of ketones to aromatic and aliphatic aldehydes is rep...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...
A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butyl...