Diastereoselectivity in the addition of grignard reagents to ketones controlled by the 1,3-dithiane 1-oxide asymmetric building block
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides
2. Stereoselective reductions of 2-keto sulfoxides with hydrides
3. Perkin communications. Diastereoselective alkylation of ketone enolates using a 1,3-dithiane 1-oxide auxiliary
4. Diastereoselective control of enolate alkylation in 2-acyl-2-alkyl-1,3-dithiane 1-oxides
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2. Cyanuric chloride-catalyzed thioacetalization for organocatalytic synthesis of thioacetals;Phosphorus, Sulfur, and Silicon and the Related Elements;2016-03-25
3. Silica Phenyl Sulfonic Acid as a Solid Acid Heterogeneous Catalyst for Chemoselective Thioacetalization of Carbonyl Compounds and Dethioacetalization under Mild Conditions;Journal of Heterocyclic Chemistry;2013-02
4. Dithioacetalization of carbonyl compounds under catalyst-free condition;Journal of Sulfur Chemistry;2011-10-20
5. Enantioselective Vanadium-Catalyzed Oxidation of 1,3-Dithianes from Aldehydes and Ketones using β-Amino Alcohol Derived Schiff Base Ligands;Advanced Synthesis & Catalysis;2011-06-30
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