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Configurational assignment of 2‐alkylsulphinyl‐1‐arylethanol diastereomers by 13 C NMR
Author(s) -
Alcudia F.,
Fernández I.,
Llera J. M.,
Trujillo M.,
Zorrilla F.
Publication year - 1988
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.1260260810
Subject(s) - chemistry , diastereomer , stereochemistry , carbon 13 nmr , proton nmr
The relative configurations of erythro ‐ and threo ‐2‐alkylsulphinyl‐1‐phenyl(or 2‐thiophen or 2‐furyl)ethanol have been correlated with 13 C NMR data. A general rule for determining the configuration of this type of compound is presented.