Structure determination of di‐ O ‐benzylidene derivatives of  L ‐iditol by  1 H and  13 C NMR spectroscopy | Zendy

Sohár P. | Zendy; Fehér G. | Zendy; Toldy L. | Zendy

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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.

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