Mild deprotection of methoxymethyl, methylthiomethyl, methoxyethoxymethyl, and and β-(trimethylsilyl,)ethoxymethyl, esters with magnesium bromide in ether
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Acid protecting group
2. Protection of carboxylic acids as methylthiomethyl esters
3. Oxidative and methylative deprotection of methylthiomethyl esters
4. Selective removal of tetrahydropyranyl ethers in the presence of tert-butyldimethylsilyl ethers with magnesium bromide in ether
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1. Facile methylthiomethylation of the carboxylic acid with bromodimethylsulfonium bromide;Green Synthesis and Catalysis;2022-08
2. Autocatalytic methylthiomethylation of carboxylic acid/phenol involving the formation of DMSO enolate: convenient synthesis of methylthiomethyl ester/ether;RSC Advances;2022
3. Synthesis of Methylthiomethyl Esters by the Reaction of Carboxylic Acid with Dimethylsulfoxide;Bulletin of the Korean Chemical Society;2018-07
4. Inverconversion of Nitriles, Carboxylic Acids, and Derivatives;Comprehensive Organic Transformations;2018-02-28
5. Fe 2 O 3 -catalyzed Pummerer rearrangement of acyl chlorides and sulfoxides: Facile synthesis of alkylthiomethyl ester;Tetrahedron Letters;2017-06
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