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Complete assignment and conformational studies of tomatine and tomatidine
Author(s) -
Willker W.,
Leibfritz D.
Publication year - 1992
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260300713
Subject(s) - chemistry , heteronuclear molecule , homonuclear molecule , aglycone , two dimensional nuclear magnetic resonance spectroscopy , glycosidic bond , nuclear overhauser effect , stereochemistry , nmr spectra database , spectral line , moiety , nuclear magnetic resonance spectroscopy , crystallography , molecule , glycoside , organic chemistry , enzyme , physics , astronomy
Abstract Heteronuclear correlation techniques and homonuclear E.COSY spectra were used to obtain a complete assignment of the 13 C and 1 H NMR spectra of the aglycone tomatidine. In addition, 1D/2D TOCSY, NOESY and ROESY spectra allowed the assignment of the sugar moiety in tomatine. The procedure used is of general applicability for the structural elucidation of sugars and glycosidic biomolecules.

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