NMR Study on 1,2,4,5-Tetrasubstituted 3,3,6,6-Tetradeuterated Cyclohexanes: Conformational Contributions and 1,3-Diaxial and Vicinal Deshielding Effects of Amino and Alkylated Amino Groups and Their Protonated Forms-Reference-Cited by-同舟云学术

NMR Study on 1,2,4,5-Tetrasubstituted 3,3,6,6-Tetradeuterated Cyclohexanes: Conformational Contributions and 1,3-Diaxial and Vicinal Deshielding Effects of Amino and Alkylated Amino Groups and Their Protonated Forms

Published:1973-05 Issue:5 Volume:62 Page:728-737
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Whelton Bartlett D.,Carr John B.,Lowry Betty R.,Huitric Alain C.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference23 articles.

1. Configurational and conformational analysis

2. Solvent effects in conformational analysis of 4-hydroxycyclohexanone

3. NMR Conformational analysis of 4-hydroxycyclohexanone and 1,4-cyclohexanediols. Coupling constants averaging induced by conformational equilibria and by strong coupling effects—role of solvent

4. Conformational analysis of 4-hydroxycyclohexanone oxime by NMR spectroscopy

5. NMR 1,3 Dialxial Deshielding Effect of the Hydroxyl Group on Ring Hydrogens Studied from Partially Deuterated Six-Membersed Ring Compunds

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4. Cyclohexane-Based Conformationally Controlled Crowns and Podands;Mini-Reviews in Organic Chemistry;2005-07-01

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