THE USE OF NAFION-H® AS AN EFFICIENT CATALYST FOR THE DEPROTECTION OF TRIMETHYLSILYL ETHERS TO THEIR CORRESPONDING ALCOHOLS UNDER MILD AND HETEROGENEOUS CONDITIONS
Author:
Affiliation:
1. a Chemistry Department, College of Science, Bu-Ali Sina University , Hamadan, Iran
2. b Department of Chemistry, Isfahan University , Isfahan, Iran
3. c Department of Chemistry, College of Science, Yazd University , Yazd, Iran
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426500490474996
Reference39 articles.
1. A Novel and Convenient Chemoselective Deprotection Method for Both Silyl and Acetyl Groups on Acidic Hydroxyl Groups Such as Phenol and Carboxylic Acid by Using a Nitrogen Organic Base, 1,1,3,3-Tetramethylguanidine
2. Facile Cleavage of Triethylsilyl (TES) Ethers Using o-Iodoxybenzoic Acid (IBX) without Affecting tert-Butyldimethylsilyl (TBS) Ethers
3. A New, Simple, and Selective Palladium-Catalyzed Cleavage of Triethylsilyl Ethers
4. Tetrabutylammonium Tribromide (TBATB)−MeOH: An Efficient Chemoselective Reagent for the Cleavage of tert-Butyldimethylsilyl (TBDMS) Ethers
5. Novel Deprotection of SEM Ethers: A Very Mild and Selective Method Using Magnesium Bromide
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