Studies of regio- and stereoselectivity in some nucleophilic ring opening reactions of N-tosyl-3-phenyl-2-aziridinemethanols and derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Regioselective nucleophilic ring opening of 2,3-aziridino alcohols
2. Enantioselective routes toward 1β-methylcarbapenems from chiral aziridines
3. Stereocontrolled synthesis via chiral aziridines
4. Chirale Aziridine — Herstellung und stereoselektive Transformationen
5. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
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1. Aziridine-2-carboxylates: Preparation, Nucleophilic Ring Opening, and Ring Expansion;HETEROCYCLES;2012
2. Electronic and chelation effects on the unusual C2-methylation of N-(para-substituted)phenylaziridines with lithium organocuprates;Journal of Computational Chemistry;2011-03-31
3. Asymmetric catalytic aziridination of dihydronaphthalenes for the preparation of substituted 2-aminotetralins;Tetrahedron;2010-12
4. Synthesis of novel N-aminoethyl cyclic polyamines;Chinese Journal of Chemistry;2010-08-27
5. ChemInform Abstract: Studies of Regio- and Stereoselectivity in Some Nucleophilic Ring Opening Reactions of N-Tosyl-3-phenyl-2-aziridinemethanols and Derivatives.;ChemInform;2010-08-17
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