Secondary Trimethylsilyl Ethers Research Articles

Silica chromate as an oxidising agent for the chemoselective oxidation of alcohols and the oxidative deprotection of trimethylsilyl ethers

Silica chromate easily converts primary and secondary alcohols to corresponding carbonyl compounds in the presence of wet SiO 2 both in dichloromethane and under solvent-free conditions at room temperature with good to excellent yields. Primary and secondary trimethylsilyl ethers were converted into the corresponding carbonyl compounds or alcohols by using silica chromate and wet SiO 2 in dichloromethane at room temperature with good to excellent yields

Zeolite‐Supported Chromium(VI) Oxide: A Mild, Efficient, and Inexpensive Reagent for Oxidative Deprotection of Trimethylsilyl Ethers under Microwave Irradiation.

Primary and secondary trimethylsilyl ethers are effeciently converted to the corresponding carbonyl compounds using HZSM-5 zeolite-supported CrO 3 under microwave irradiation in solventless system.

Oxidative Deprotection of Trimethylsilyl Ethers Using Bismuth Nitrate Supported onto Montmorillonite k‐10 under Microwave Irradiation in Solventless System.

AbstractFor Abstract see ChemInform Abstract in Full Text.

ZEOLITE-SUPPORTED CHROMIUM(VI) OXIDE: A MILD, EFFICIENT, AND INEXPENSIVE REAGENT FOR OXIDATIVE DEPROTECTION OF TRIMETHYLSILYL ETHERS UNDER MICROWAVE IRRADIATION

Primary and secondary trimethylsilyl ethers are effeciently converted to the corresponding carbonyl compounds using HZSM-5 zeolite-supported CrO 3 under microwave irradiation in solventless system.

Oxidative Deprotection of Trimethylsilyl Ethers using Bismuth Nitrate Supported onto Montmorillonite k-10 under Microwave Irradiation in Solventless System

Primary and secondary trimethylsilyl ethers are converted to their carbonyl compounds efficiently using montmorillonite k-10 supported bismuth nitrate under microwave irradiation in a solventless system.

A Rapid Method for Oxidative Deprotection of Trimethylsilyl Ether with Wet Alumina Supported Dess—Martin Periodinane in Solventless System under Microwave Irradiation.

AbstractFor Abstract see ChemInform Abstract in Full Text.

Silica Sulfuric Acid: An Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to Their Corresponding Ethers under Mild and Heterogeneous Conditions.

AbstractFor Abstract see ChemInform Abstract in Full Text.

The Use of Nafion‐H® as an Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to Their Corresponding Ethers under Mild and Heterogeneous Conditions.

Primary and secondary trimethylsilyl ethers were converted to their corresponding ethers in the presence Nafion-H® with good to excellent yields under mild and heterogeneous conditions.

Quinulinium Fluorochromate C9H7NHCrO3F: An Efficient and Convenient Reagent for the Oxidative Deprotection of Trimethylsilyl Ethers in Non-Aqueous Conditions

Primary and secondary trimethylsilyl ethers are efficiently converted to their carbonyl compound using quinolinium fluorochromate in nonaqueous conditions.

The use of Nafion-H® as an efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions

Primary and secondary trimethylsilyl ethers were converted to their corresponding ethers in the presence Nafion-H® with good to excellent yields under mild and heterogeneous conditions.

Efficient and Selective Oxidative Deprotection of Trimethylsilyl Ethers Using Supported Potassium Ferrate Under Microwave Irradiation

Primary and secondary trimethylsilyl ethers are efficiently and rapidly converted to their corresponding carbonyl compounds with supported potassium ferrate under microwave irradiation in solventless system.

Silica Sulfuric Acid: An Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to their Corresponding Ethers under Mild and Heterogeneous Conditions

Primary and secondary trimethylsilyl ethers were converted to their corresponding ethers in the presence silica sulfuric acid with good to excellent yields under mild and heterogeneous conditions.

Direct Oxidative Deprotection of Trimethylsilyl Ethers to their Corresponding Carbonyl Compounds with Bis (trimethylsilyl) Chromate Supported onto Silica Gel in Aprotic Solvent

Primary and secondary trimethylsilyl ethers are converted to their carbonyl compounds effeciently using bis (Trimethylsilyl) chromate supported on silica gel in dichloromethane. Benzylic double bonds are not prone to cleavage reactions with this method.

Direct Conversion of Secondary Trimethylsilyl Ethers to Ketones

Direct Conversion of Secondary Trimethylsilyl Ethers to Ketones