Magnesium Bromide Mediated Selective Conversion of Acetals into Thioacetals
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/18/4/18_4_629/_pdf
Reference8 articles.
1. Selective protection of carbonyl compounds. Silica gel treated with thionyl chloride as an effective catalyst for thioacetalization
2. Selective removal of tetrahydropyranyl ethers in the presence of tert-butyldimethylsilyl ethers with magnesium bromide in ether
3. Synthetic applications of metal halides. Conversion of cyclopropylmethanols into homoallylic halides
4. Cleavage of cyclic ethers by magnesium bromide-acetic anhydride. SN2 substitution at a secondary site
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1. Protection for the Carbonyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. Highly efficient and chemoselective method for the thioacetalization of aldehydes and transthioacetalization of acetals and acylals catalyzed by H2SO4-silica under solvent-free conditions;Monatshefte für Chemie - Chemical Monthly;2011-11-09
3. Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide as a mild and efficient catalyst for chemoselective thioacetalization of carbonyl functions and transthioacetalization reactions;Journal of Heterocyclic Chemistry;2011-02-22
4. An Efficient Method for the Transthioacetalization of Acylals and Acetals under Mild Conditions;E-Journal of Chemistry;2011
5. A Novel Approach to the Practical Synthesis of Sulfides: An InBr3-Et3SiH Catalytic System Promoted the Direct Reductive Sulfidation of Acetals with Disulfides;European Journal of Organic Chemistry;2009-08
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