Proton magnetic resonance studies of specifically deuterated cyclohexane compounds. Part IV. 1,1-Dimethylcyclohexane, 1,3- and 1,4-di-t -butylcyclohexane (cis and trans ), and cis,cis -1,3,5-tri-t -butylcyclohexane-Reference-Cited by-同舟云学术

Proton magnetic resonance studies of specifically deuterated cyclohexane compounds. Part IV. 1,1-Dimethylcyclohexane, 1,3- and 1,4-di-t -butylcyclohexane (cis and trans ), and cis,cis -1,3,5-tri-t -butylcyclohexane

Published:1974 Issue:4 Volume:93 Page:93-98
ISSN:0165-0513
Container-title:Recueil des Travaux Chimiques des Pays-Bas
language:en
Short-container-title:Recl. Trav. Chim. Pays-Bas

Author:

Remijnse J. D.,van Bekkum H.,Wepster B. M.

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19740930402/fullpdf

Reference19 articles.

1. Anomalous Chemical Shifts in the Proton Magnetic Resonance Spectra of the Dimethylcyclohexanes and Related Hydrocarbons

2. “Anomalous” Chemical Shifts in the Nuclear Magnetic Resonance Spectra of the 1,3,5-Trimethylcyclohexanes

3. Geometry of the substituted cyclohexane ring

4. H. Booth P. R. Thornburrow J. Chem. Soc. B. 1971 1051

5. Conformation of non-aromatic ring compounds

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4. Cyclohexylene-Bridged Porphyrin Quinones with Variable Acceptor Strength as Biomimetic Models for Photosynthesis: Evidence for Twist-Boat Conformation;The Journal of Organic Chemistry;1997-12-01

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