p-Toluenesulfonyl Chloride (p-TsCl)-Catalyzed Trimethylsilylation of Hydroxyl Groups Using Hexamethyldisilazane and Their Regeneration Under Mild Conditions: The First Example for Catalytic Application of p-Toluenesulfonyl Chloride
Author:
Affiliation:
1. a Faculty of Chemistry , Bu-Ali Sina University , Hamadan, Iran
2. b Department of Chemistry, Faculty of Science , University of Kurdistan , Sanandaj, Iran
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426500802453872
Reference35 articles.
1. Protective Groups in Organic Synthesis
2. Protecting groups
3. An efficient method for the trimethylsilylation of tertiary alcohols
4. Synthesis methods and reactions. 71. Chlorotrimethylsilane and tert-butyl dimethylsilyl chloride/lithium sulfide, mild and efficient silylating reagents
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1. Synthetic applications of p-toluenesulfonyl chloride: A recent update;Journal of Molecular Structure;2023-10
2. Cu(NO3)2 · 3 H2O as an Efficient Reagent for the Chemoselective Trimethylsilylation of Primary Alcohols and Oxidation of Trimethylsilyl Ethers;Phosphorus, Sulfur, and Silicon and the Related Elements;2012-01-31
3. p-Toluenesulfonyl chloride as a new and effective catalyst for acetylation and formylation of hydroxyl compounds under mild conditions;Chinese Chemical Letters;2010-12
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