Preference for Eclipsed Conformations in Acyclic Neopentyldialkylamines and the Stereodynamical Consequences: An NMR and Molecular Mechanics Investigation1-Reference-Cited by-同舟云学术

Preference for Eclipsed Conformations in Acyclic Neopentyldialkylamines and the Stereodynamical Consequences: An NMR and Molecular Mechanics Investigation1

Published:1997-08-01 Issue:34 Volume:119 Page:8050-8057
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Anderson J. Edgar¹,Casarini Daniele¹,Ijeh Anthony I.¹,Lunazzi Lodovico¹

Affiliation:

1. Contribution from the Chemistry Department, University College, Gower Street, London WC1 E6BT, U.K., and Department of Organic Chemistry “A. Mangini”, University of Bologna, Viale Risorgimento 4, Bologna 40136, Italy

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9710363

Reference36 articles.

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3. (b) Dhar, R. K.; Sygula, A.; Fronczek, F. R.; Rabideau, P. W.Tetrahedron1992,48, 9417.

4. 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

5. 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

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