Stereodynamics of N-Isopropyl-N-methylpropargylamine. Dynamic NMR Studies. Molecular Mechanics Calculations
Author:
Affiliation:
1. Science Department/Chemistry Program, Southwest State University, Marshall, Minnesota 56258
2. Chemistry Department, University of Vermont, Burlington, Vermont 05405
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo001389b
Reference37 articles.
1. Stereodynamics of N-tert-butyl-N,N-dialkylamines. Experimental and theoretical evidence for a common potential surface for tert-butyl rotation and nitrogen inversion
2. Amino wagging and inversion in methylamines
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1. Interplay of Nitrogen-Atom Inversion and Conformational Inversion in Enantiomerization of 1H-1-Benzazepines;The Journal of Organic Chemistry;2016-03-29
2. Partial rotation of the isopropyl group in the solid state: single-crystal-to-single-crystal phase transformation in a carvacrol derivative;CrystEngComm;2015
3. Recent Advances in Stereodynamics and Conformational Analysis by Dynamic NMR and Theoretical Calculations;European Journal of Organic Chemistry;2010-03-26
4. N-Inversion-Associated Conformational Dynamics Is Unusually Rapid in Morphine Alkaloids;Journal of Natural Products;2004-10-29
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