Hydrazin‐Reaktionen, X Untersuchungen an inversionsisomeren 1‐Chlor‐und 1‐Amino‐aziridinen Abhängigkeit der 1 H–C– 14 N‐Kopplung von der Konformation des freien Elektronenpaares
Author:
Affiliation:
1. Aus dem Institut für Organische Chemie der Universität Hamburg
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19701030218
Reference44 articles.
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3. Aziridines from Diazomethane and Fluorine-Substituted Imines
4. Measurement of the Inversion Rate of a Secondary Amine and Its N-Deuterio Analog by Nuclear Magnetic Resonance Spectroscopy1
5. Nuclear Magnetic Resonance Spectra and Nitrogen Inversion in 1-Acylaziridines
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1. Aziridines;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Preparation of racemic 2,3-diaminobutane and the resolution of its (2S,3S) enantiomer;Tetrahedron: Asymmetry;1997-05
3. Convenient procedure for converting 1,3-dithiolane-2-thiones into 1,3-dithiolan-2-ones;Journal of the Chemical Society, Perkin Transactions 1;1996
4. NMR spectral parameters of 1-chloroaziridine;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1990-02
5. Optically active trifluoromethylcarbinols as chiral solvating agents for asymmetric transformations at a ring-nitrogen atom. Synthesis of optically active N-chloroaziridines and stereochemical aspects of chiral solvent-aziridine solute complexes;The Journal of Organic Chemistry;1983-08
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