## Abstract The ^13^C‐NMR. spectra of one natural and ten semi‐synthetic cannabinoids were analyzed in detail. Assignments of the signals are based on their chemical shifts, splitting patterns in ^1^H‐off‐resonance decoupling experiments and comparison with ^13^C‐NMR. data of related cannabinoids.
Re-examination of the 13C NMR spectra of synthetic chlorins
✍ Scribed by Alan M. Stolzenberg; Matthew T. Stershic
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 346 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 13C NMR spectra of the synthetic chlorins H,(OEC), Ni(TMC) and H,(TPC) have been re-examined. Evidence from single-frequency proton decoupled, proton coupled, and 2D 13C-13C INADEQUATE experiments show that the previous assignments of the meso-substituted chlorins were incorrect. Corrected assignments establish that the a-pyrroline carbons of chlorins occur at lower fields (150-175 ppm) than the a-pyrrole carbons.
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