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Structure determination of di‐ O ‐benzylidene derivatives of L ‐iditol by 1 H and 13 C NMR spectroscopy
Author(s) -
Sohár P.,
Fehér G.,
Toldy L.
Publication year - 1981
Publication title -
organic magnetic resonance
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0030-4921
DOI - 10.1002/mrc.1270150205
Subject(s) - hydrolysis , nuclear magnetic resonance spectroscopy , chemistry , derivative (finance) , product (mathematics) , spectroscopy , stereochemistry , organic chemistry , physics , mathematics , geometry , quantum mechanics , financial economics , economics
The configuration and stable conformation of two dibenzylidene‐ L ‐iditol isomers formed upon benzalation of L ‐iditol, as well as that of a third isomer obtained by partial hydrolysis of the tribenzylidene derivative—the main product of the benzalation reaction—were determined by 1 H and 13 C NMR spectroscopy.