ISSN:
0749-1581
Keywords:
Cedrane derivatives
;
lac acids
;
2,6,6,8-tetramethyltricyclo-[5.3.11,7.O1,5]undecane
;
conformational analysis
;
Chemistry
;
Analytical Chemistry and Spectroscopy
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The complete analysis of the 13C NMR spectra of 30 cedrane derivatives with various functionalities on the 2, 6, 6, 8-tetramethyltricyclo[5.3.11,701,5]undecane skeleton is reported. The assignment of the signals to the appropriate carbons has been made using the various functionalities on the molecular framework and the chemical shift theory (α, β, γ effects). When necessary, off-resonance decoupling, INEPT and DEPT experiments have been used, as well as specific deuterium labelling. The last ambiguities were resolved with the aid of lanthanide shift reagents and SFORD experiments. The assignments for the reference compounds neoisocedranol oxide, cedrol and cedrene were made using the carbon-carbon connectivity 2D INADEQUATE pulse sequence. The examination of cedrane derivatives functionalized on C-9 (carbonyl, hydroxyl, acetate) and C-8 (methyl, axial or equatorial) showed that the 13C chemical shifts of C-5, -6, -11 and -13 are sensitive probes for the conformation of the six-membered ring (ring C), which is essentially a flattened chair, and for the stereochemistry of the C-8 and C-9 substituents. Comparison with 2-methylbicyclo[3.2.1]octan-3-ones shows that the Anti Reflex effect is operative in cedrane derivatives.Cedrane oxides and their derivatives have also been examined and the corresponding 13C data are reported. Using all this information it was possible to carry out a complete analysis of lac acids, which have a functionalized tricyclo[5.31,7, 01,5]undecane framework like the cedrane derivatives. The 13C spectral analysis shows that, from the structural point of view, this tricyclic system behaves as a bicyclo[3.3.0] skeleton with an additional three-carbon bridge between C-1 and C-7, rather than as a bicyclo[3.2.1]octane with an additional cyclopentane fused on C-1 and C-5; when additional strain is introduced into this system, the five-membered ring A and the six-membered ring C undergo conformational deformations more easily than ring B.
Additional Material:
4 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/mrc.1260250713
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