A Superstable Nitrogen Pyramid: Stereodirected N-Halogenation of Methyl 2-Aziridinecarboxylate
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference14 articles.
1. Influence of steric factors on the rates of thermal racemisation of N-alkyl-oxaziridines. Isolation of an enantiomer whose optical activity is due solely to a tercovalent asymmetric nitrogen atom
2. Configurational stability of pyramidal nitrogen in spiro-oxaziridines
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1. Stereodynamics of Nitrogen Chiral Centers in aza-β3 -Cyclodipeptides;Chirality;2013-05-09
2. Aza-β 3 -cyclopeptides: A New Way of Controlling Nitrogen Chirality;Journal of the American Chemical Society;2009-09-16
3. Synthesis and stereodirected N-halogenation of trans-3-trifluoromethyl-2-methoxycarbonylaziridine;Journal of Fluorine Chemistry;1998-05
4. N-Fluorination of aziridinecarboxylates via fluorolysis of their N-aminomethyl derivatives;Mendeleev Communications;1998-01
5. Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side;Mendeleev Communications;1997-01
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