2001
DOI: 10.1201/9780203908389.ch10
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Solid-State Nuclear Magnetic Resonance Spectroscopy

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Cited by 13 publications
(32 citation statements)
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“…13 C CPMAS NMR would result in prohibitively long measuring times in our case. Therefore, we undertook 13 C labeling of those 13 C nuclei, which give resonances diagnostic for the crystal form in solid-state 13 C CPMAS NMR. Org OD 14 was labeled both at the 19-and 20-ethynyl and the 21-methyl positions as indicated in Figure 1.…”
Section: Introductionmentioning
confidence: 95%
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“…13 C CPMAS NMR would result in prohibitively long measuring times in our case. Therefore, we undertook 13 C labeling of those 13 C nuclei, which give resonances diagnostic for the crystal form in solid-state 13 C CPMAS NMR. Org OD 14 was labeled both at the 19-and 20-ethynyl and the 21-methyl positions as indicated in Figure 1.…”
Section: Introductionmentioning
confidence: 95%
“…The 13 C labeling of Org OD 14 was carried out as reported elsewhere. 15 Mass spectrometric analysis showed an isotope incorporation of >95%.…”
Section: Labelingmentioning
confidence: 99%
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“…Because of its strength in the characterization of pharmaceutical formulations, solid-state NMR spectroscopy was chosen as the primary analytical technique to characterize PDL in the solid state following different formulation conditions. [20][21][22][23][24][25][26][27][28][29][30] The objective of this research was to investigate the effects of formulation and processing variables on PDL in the solid state. The parameters studied included mixing time, water, drying conditions, and excipient ratios.…”
mentioning
confidence: 99%