NMR Study on Oxazolidne Derivatives of 1,4:3,6-Dianhydro-D-Fructose
Hong‐Min Liu
Abstract
Hong‐Min Liu
Abstract
In this study,some new oxazolidine derivatives were prepared from 1,4:3,6-dianhydro-D-fructose.Because of many same structural units in these compounds,the chemical environment of these compounds was extremely similar.The structures of these oxazolidines were evaluated with 1D and 2D NMR spectroscopy(1H NMR,13C NMR,DEPT-135,1H-1H COSY,HSQC,HMBC) and HRMS spectra.1H NMR and 13C NMR chemical shifts of these compounds were assigned.The stereochemistry of these compounds was established by the results obtained from X-ray crystal analysis of the relative compounds and NOESY spectroscopy.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
In this study,some new oxazolidine derivatives were prepared from 1,4:3,6-dianhydro-D-fructose.Because of many same structural units in these compounds,the chemical environment of these compounds was extremely similar.The structures of these oxazolidines were evaluated with 1D and 2D NMR spectroscopy(1H NMR,13C NMR,DEPT-135,1H-1H COSY,HSQC,HMBC) and HRMS spectra.1H NMR and 13C NMR chemical shifts of these compounds were assigned.The stereochemistry of these compounds was established by the results obtained from X-ray crystal analysis of the relative compounds and NOESY spectroscopy.
Key concepts: DEPT, Heteronuclear single quantum coherence spectroscopy, Two-dimensional nuclear magnetic resonance spectroscopy, Chemistry, Carbon-13 NMR, Nuclear magnetic resonance spectroscopy, Chemical shift, Proton NMR