Abstract
The13C NMR spectra of the initial ω-aryloxy chains and the final 16-and 17-aryloxyprostaglandins of the 11-deoxy series have been investigated, and stereochemical assignments have been made for the diastereomeric pairs. A weakening of the diastereotopic effects in the spectra of the 15- and 16-methyl-substituted 16- and 17-phenoxypropstaglandins to 0.1 ppm has been shown.
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