Preparation of Nano Silica Supported Sodium Hydrogen Sulfate: As an Efficient Catalyst for the Trimethyl, Triethyl and<i>t</i>-Butyldimethyl Silylations of Aliphatic and Aromatic Alcohols in Solution and under Solvent-free Conditions
作者:Abdolreza Abri、Somayeh Ranjdar
DOI:10.1002/jccs.201300586
日期:2014.8
Nano silicasupportedsodiumhydrogensulfate has been prepared by mixing NaHSO4 with activated Nano silicagel. We wish to report a new method for the synthesis of trimethyl (TMS), triethyl (TES) and t‐butyldimethyl silyl (TBS) ethers from benzylic, allylic, propargylic alcohols, phenols, naphtholes and some of phenolic drugs in the solution and under solvent‐free conditions.
Novel Nickel-Catalyzed Coupling Reaction of Allyl Ethers with Chlorosilanes, Alkyl Tosylates, or Alkyl Halides Promoted by Vinyl-Grignard Reagent Leading to Allylsilanes or Alkenes
method for a carbon-silicon or carbon-carbon bond forming reaction between allyl ethers and chlorosilanes, alkyl tosylates, or alkylhalides giving rise to allylsilanes or alkenes has been developed. This reaction proceeds efficiently at ambient temperature by the combined use of nickel catalysts and a vinyl-Grignard reagent. A possible reaction pathway involving the formation of allyl-Grignard reagents
Cobalt and Manganese Salts of p -Aminobenzoic Acid Supported on Silica Gel: A Versatile Catalyst for Oxidation by Molecular Oxygen
作者:Mohammed M. Hashemi、Yusef Ahmadibeni
DOI:10.1007/s00706-002-0534-3
日期:2003.2.1
A 1:1 molar ratio of the cobalt and manganese salts of p -amino benzoic acid supported on silica gel is an effective catalyst for the oxidation of various organic compounds in reasonable yields using molecular oxygen. The catalyst can be reused several times.
Efficient and practical protocol for silylation of hydroxyl groups using reusable lithium perchlorate dispread in silica gel under neutral condition
作者:Najmedin Azizi、Rozbeh Yousefi、Mohammad R. Saidi
DOI:10.1016/j.jorganchem.2005.11.005
日期:2006.2
for the trimethylsilylation of a wide variety of alcohols, including primary, allylic, benzylic, secondary, hindered secondary, tertiary, and phenols with hexamethyldisilazane on the surface of silica gel dispersed with LiClO4 in room temperature at few minutes in excellent yields under neutral conditions is reported. This procedure also allows the excellent selectivity under LP-SiO2 system for silylation
Aluminium Triflate [Al(OTf)<sub>3</sub>] as a Recyclable Catalyst for the Conversion of α-Hydroxyphosphonates, Alcohols and Phenols to Their Corresponding O-Silylated Products with Hexamethyldisilazane (HMDS)
Al(OTf)3 as a recyclable catalyst conducts the efficient conversion of various types of α-hydroxyphosphonates to their corresponding α-trimethysilyloxyphosphonates with HMDS in the absence of solvent at room temperature. The general applicability of the catalyst under solvent-free conditions is demonstrated by applying it for the successful silylation of alcohols and phenols with HMDS in high yields.