Structural characterization of (±)-N-chloro-2,2-bis(methoxycarbonyl)aziridine by X-ray crystallography and 2D NMR spectroscopy
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1992/P2/P29920001541
Reference21 articles.
1. Optically active N-chloro-2,2-bismethoxycarbonylaziridine by enzymatic hydrolysis.
2. Optically active cis- and trans-1-chloro-2-methoxycarbonyl-2-methylcarbamoylaziridines. Stereochemical properties
3. Relationships between solid-state structures of enantiomers and the corresponding racemic compounds in small ring derivatives. Comparison of crystal structures and solid-state properties of (R)-(–)- and racemic 1-chloro-2,2-diphenylaziridine. Solvent effect on the racemization of (R)-(–)-1-chloro-2,2-diphenylaziridine
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1. Acyl migration from N to C in aziridine-2-carboxylic esters;Tetrahedron;2014-01
2. ChemInform Abstract: Structural Characterization of (.+-.)-N-Chloro-2,2-bis(methoxycarbonyl) aziridine by X-Ray Crystallography and 2D NMR Spectroscopy;ChemInform;2010-09-01
3. Aziridine-2-carboxylic Acid;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side;Mendeleev Communications;1997-01
5. Derivatives of 1-fluoroaziridine-2,2-dicarboxylic acid;Mendeleev Communications;1997-01
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