13C nuclear magnetic resonance spectra of 23-hydroxy spirostane sapogenins of Solanum hispidum
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چکیده
منابع مشابه
Nuclear magnetic resonance spectroscopy: 13C spectra of unsubstituted inositols.
The chemical shifts of (13)C in natural abundance have been obtained from nuclear magnetic resonance spectra of scyllo-, myo-, chiro-, and epi-inositols at 15.1 MHz. A set of empirical substitutent parameters were derived and shown to be moderately successful in correlating the (13)C resonance-line positions for these substances. The substituent parameters conform generally to the idea that ste...
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The 13C resonance spectra of fungal melanins from Aspergillus niger, Eurotium echinolatum, and Stachybotrys chartarum are reported. The spectra were taken in 5% W/W solution of the substances in 0.1 N NaOD in D2O using the Fourier-transform-technique. The spectra and possible assignments of the bands are discussed. The similarities of these spectra to those of soil humic acids are unexpectedly ...
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~3C and 295i nuclear magnetic resonance spectroscopy with magic-angle spinning bas been used to study the short-range ordering and bonding in the structures of intercalates of kaolinite with formamide, hydrazine, dimethyl sulfoxide (DMSO), and pyridine-N-oxide (PNO). The 29Si chemical shift indicated decreasing levels of bonding interaction between the silicate layer and the intercalate in the ...
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Natural-abundance (13)C nuclear magnetic resonance spectra are reported for some simple terpenes and carotenes. The techniques involved in the assignment of the resonances to specific carbons are outlined. The potential of this nondegradative procedure for structural analysis is demonstrated for the investigation of carbon atoms in chemical and biochemical systems.
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Study of the nuclear magnetic resonance spectra of glyoxaldihydrazone in dimethylsulfoxide and deuterochlorofonn leads to the conclusion that this compound exists predominantly in non-chelate structure
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ژورنال
عنوان ژورنال: Canadian Journal of Chemistry
سال: 1981
ISSN: 0008-4042,1480-3291
DOI: 10.1139/v81-195