Eclipsed Conformation of the Exocyclic N−CH2 Bond in N-Neopentylpiperidines and the Stereodynamic Consequences As Studied by Dynamic NMR Spectroscopy and Molecular Mechanics Calculations-Reference-Cited by-同舟云学术

Eclipsed Conformation of the Exocyclic N−CH2 Bond in N-Neopentylpiperidines and the Stereodynamic Consequences As Studied by Dynamic NMR Spectroscopy and Molecular Mechanics Calculations

Published:1998-04-30 Issue:10 Volume:63 Page:3310-3317
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Anderson J. Edgar,Ijeh Anthony I.,Storch Christine,Casarini Daniele,Lunazzi Lodovico

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9720344

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3. Conformational analysis of 1,3-dioxanes with sulfide, sulfoxide and sulfone substitution at C(5). Finding an eclipsed conformation in cis-2-tert-butyl-5-(tert-butylsulfonyl)-1,3-dioxane

4. Conformational analysis of 5-substituted 1,3-dioxanes. 5. Bond eclipsing in tert-butylsulfonyl substituted 1,3-dioxanes and cyclohexanes. X-ray diffraction studies, MMP2 calculations, and interpretation

5. Conformation and stereodynamics of a highly hindered ethane, 1,2-bis(2,4,6-tri-tert-butylphenyl)ethane, and of the corresponding ethyl radical

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