ISSN:
1434-4475
Keywords:
Configurational correlation
;
5-Ethylindanes
;
1 H-nmr spectra
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract Starting from (+) (2R) methyl 5′-ethyl-2,2′-spirobiindane-5-carboxylate of known enantiomeric purity 79 optically active, configurationally correlated 5,5′,6′-trisubstituted 2,2′-spirobiindanes (2–7) were prepared for the purpose of testing a “shortened polynomal Ansatz” for chirality functions. Their optical rotations and1H-nmr spectra are reported. In this context several 6-substituted 5-ethylindanes (1) were prepared as model compounds for synthetic transformations.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00938359
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