2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO), N-Bromosuccinimide (NBS) and Bromine as Efficient Catalysts for Dithioacetalization and Oxathioacetalization of Carbonyl Compounds and Transdithioacetalization Reactions
作者:Nasser Iranpoor、Habib Firouzabadi、Hamid Reza Shaterian、M. A. Zolfigol
DOI:10.1080/10426500211712
日期:2002.5.1
6-tetrabromo-2,5-cyclohexadienone (TABCO), N-bromosuccinimide (NBS), and bromine as efficient catalysts for conversion of carbonyl compounds to their cyclic and acyclic dithioacetals and 1,3-oxathiolanes under mild reaction conditions are described. These catalysts are also used for efficient transdithioacetalization of acetals, diacetals, ketals, acylals, enamines, hydrazones, and oximes with high
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.
Indium Tribromide as a Highly Efficient and Versatile Catalyst for Chemoselective Synthesis of Acylals from Aldehydes under Solvent-Free Conditions
作者:Yong-Mei Wang、Liang Yin、Zhan-Hui Zhang、Mei-Li Pang
DOI:10.1055/s-2004-829549
日期:——
A mild and efficient method has been developed for the chemoselective preparation of acylals from aldehydes in the presence of catalytic amounts (0.01-1.0 mol%) of InBr3 under solvent-free conditions in very good to excellent yields.
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