Nuclear Magnetic Resonance Spectra. Nitrogen Inversion Rates of N-Substituted Aziridines (Ethylenimines) 1
AT Bottini, JD Roberts
Index: Bottini; Roberts Journal of the American Chemical Society, 1958 , vol. 80, p. 5203,5208
Full Text: HTML
Citation Number: 138
Abstract
In 1939, several groups of workers? postulated iiideperidently that suitably substituted aziridines (ethylenimines) might be favorably constituted to permit existence of stable, optically active antipodes. This idea was given support by Kincaid and Henriquesj through calculations of the magni-
Related Articles:
[Schloegl,K.; Schloegl,R. Monatshefte fuer Chemie, 1964 , vol. 95, p. 922 - 941]
[Goldberg; Whitmore Journal of the American Chemical Society, 1937 , vol. 59, p. 2280]
[Schmidt; Schmidt, Brigitte F.; Snyder; Snyder, Emily J.; Carroll; Carroll, Robin M.; Farnsworth; Farnsworth, David W.; Michejda; Michejda, Christopher J.; Smith R.H.; Smith Jr., Richard H. Journal of Organic Chemistry, 1997 , vol. 62, # 25 p. 8660 - 8665]