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.
New Applications of Solid Silica Chloride (SiO 2 -Cl) in Organic Synthesis. Efficient Preparation of Diacetals of 2,2-Bis(Hydroxymethyl)-1,3-propanediol from Different Substrates and Their Transthioacetalization Reactions. Efficient Regeneration of Carbonyl Compounds from Acetals and Acylals
application of solid silica chloride, an easily available and efficient catalyst for the preparation of diacetal of 2,2-bis-(hydroxymethyl)-1,3-propanediol from aldehydes, acetals, acylals, and oximes, is described. Transthioacetalization of diacetals of 2,2-bis-(hydroxymethyl)-1,3-propanediol into their corresponding 1,3-dithianes and 1,3-dithiolanes in the presence of silica chloride is presented. Efficient
Bismuth (III) Chloride<sup>1</sup>; an Efficient and Selective Catalyst for Deprotection of 1,1-Diacetates
作者:I. Mohammadpoor-baltork、H. Aliyan
DOI:10.1080/00397919908086439
日期:1999.8
Abstract A variety of 1,1-diacetates are easily and efficiently deprotected in the presence of catalytic amounts of bismuth(III) chloride affording the corresponding aldehydes in high yields.
Aluminium Chloride: A Mild and Efficient Catalyst for Selective Deprotection of 1,1-Diacetates
作者:Iraj Mohammadpoor-Baltork、Hamid Aliyan
DOI:10.1039/a807187j
日期:——
A mild, efficient and excellent yield method for the selective deprotection of 1,1-diacetates to the corresponding aldehydes in the presence of aluminium chloride (AlCl3) is described.