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. 2019 Nov 4;58(51):18540–18546. doi: 10.1002/anie.201908914

Figure 3.

Figure 3

Overlay of the 1H solid‐state NMR spectra of CUR‐11‐P, CUR‐6‐P, a physical 1:1 mixture, and as‐received CUR recorded at 14.1 T and 65 kHz MAS. The enol and the hydroxy moieties of the curcumin are indicated for the respective samples.