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Interpretation of NMR spectra from four-membered rings

✍ Scribed by Earl B. Whipple; George R. Evanega


Publisher
John Wiley and Sons
Year
1970
Tongue
English
Weight
283 KB
Volume
2
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

When as many as four vicinal couplings occur between four protons situated on three carbon atoms of a cyclobutane ring, one can employ the Karplus relation to assign the configuration of substituents at the remaining positions and make some inferences about the stereochemistry. Four examples are described; the spectra and data are analyzed.


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