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Magn Reson Chem ; 46(1): 69-74, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18098158

ABSTRACT

Using modern NMR techniques, including 1H--13C and 1H--15N heteronuclear correlation experiments, the complete and unambiguous 1H, 13C, and 15N NMR chemical shift assignments of annomontine, methoxyannomontine, and N-hydroxyannomontine pyrimidine-beta-carboline alkaloids were performed. All 1H--1H scalar coupling constants and signal multiplicities were determined, and all nOe observations were also included.


Subject(s)
Alkaloids/chemistry , Carbolines/chemistry , Magnetic Resonance Spectroscopy/methods , Pyrimidines/chemistry , Alkaloids/isolation & purification , Annona/chemistry , Carbolines/isolation & purification , Molecular Structure , Pyrimidines/isolation & purification
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