Lewis acid-catalysed rearragnement/reduction of 1-phenyloxiranemethanamines: synthesis of β-phenethylamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Highly diasteroselective intermolecular 1,3-dipolar cycloaddition reactions of carbonyl ylides with aldimines to afford sterically disfavored cis-oxazolidines;Organic Chemistry Frontiers;2014
2. Unexpected Formation of Naphtyl 1,3-Diaminopropan-2-ol Derivative through Azetidinium Ion Intermediate;Bulletin of the Korean Chemical Society;2012-11-20
3. The Use of Glycidyl Ethers Involving Aziridinium Intermediates and Other Methodology for the Preparation of Enantiomerically Pure Drug Candidates;Organic Process Research & Development;2012-01-06
4. Metallocene catalyzed synthesis of fungistatic vicinal aminoalcohols under solvent free conditions;Bioorganic & Medicinal Chemistry Letters;2010-11
5. ChemInform Abstract: Lewis Acid Catalyzed Rearrangement/Reduction of 1- Phenyloxiranemethanamines: Synthesis of β-Phenethylamines.;ChemInform;2010-08-04
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