2,6-Dicarboxypyridinium Chlorochromate. An Efficient and Selective Reagent for the Mild Deprotection of Acetals, Thioacetals, and 1,1-Diacetates to Carbonyl Compounds
chlorochromate (2,6- DCPCC ) was found to be an efficientreagent for the conversion of acetals, thioacetals, and 1,1-diacetates to their corresponding carbonyl compounds under neutral and anhydrous conditions in good to excellent yields. Selectivedeprotection of acetals or 1,1-diacetates in the presence of thioacetals at room temperature is also observed with this reagent.
Poly(4-vinylpyridinium) perchlorate as an efficient solid acid catalyst for the chemoselective preparation of 1,1-diacetates from aldehydes under solvent-free conditions
作者:Nader Ghaffari Khaligh
DOI:10.1016/s1872-2067(12)60750-5
日期:2014.3
Abstract Poly(4-vinylpyridinium) perchlorate has been used as a supported, recyclable, environmentally-benign catalyst for the formation of acylals from aliphatic and aromatic aldehydes in good to excellent yields under solvent-free conditions. Notably, the reaction conditions were tolerant of ketones. This methodology offers several distinct advantages, including its operational simplicity and high
simple and efficient procedure for the preparation of silica‐bonded propyl‐diethylene‐triamine‐N‐sulfamic acid (SPDTSA) by reaction of 3‐diethylenetriamine‐propylsilica (DTPS) and chlorosulfonic acid in chloroform is described. Silica‐bonded propyl‐diethylene‐triamine‐N‐sulfamic acid is employed as a recyclable catalyst for the synthesis of 1,1‐diacetates from aromatic aldehydes and acetic anhydride under
A simple and efficient procedure for the preparation of silica-bonded S-sulfonic acid (SBSSA) by reaction of 3-mercaptopropylsilica (MPS) and chlorosulfonic acid in chloroform is described. This solidacid is employed as a recyclablecatalyst for the synthesis of 1,1-diacetates from aromatic aldehydes and acetic anhydride under mild and solvent-free conditions at room temperature.
A succinimide-N-sulfonic acid catalyst for acetylation reactions in absence of a solvent
作者:Farhad SHIRINI、Nader Ghaffari KHALIGH
DOI:10.1016/s1872-2067(11)60499-3
日期:2013.4
Abstract A small amount of succinimide-N-sulfonic acid efficiently catalyzed the acetylation of a variety alcohols, phenols, thiols, amines and aldehydes with acetic anhydride at room temperature under solvent free conditions. This catalyst has the advantages of excellent yields and short reaction times and the reaction can be carried out on a large scale, which makes it potentially useful for industrial