Abstract
The use of chlorotrimethylsilane-sodium iodide gave excellent results in mild, neutral nonaqueous cleavage-hydrolysis reaction of C-0 bond, deoxygenation of sulfoxide and N-oxide iodonation of alcohol, and dehalogenation of α-haloketone. This reagent can be used as covenient and inexpensive alternatives for iodotrimethylsilane. © 1981, The Society of Synthetic Organic Chemistry, Japan. All rights reserved.
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CITATION STYLE
APA
Morita, T., Okamoto, Y., & Sakurai, H. (1981). Chlorotrimethylsilane-Sodium Iodide. Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 39(10), 973–977. https://doi.org/10.5059/yukigoseikyokaishi.39.973
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