## Abstract Twenty‐six new aminoflavones have been synthesised by two different methods and the structure elucidation was accomplished using extensive 1D (^1^H, ^13^C) and 2D NMR spectroscopic studies (COSY, HSQC and HMBC experiments). Copyright © 2006 John Wiley & Sons, Ltd.
Structure elucidation of a novel group of dithiocarbamate derivatives using 1D and 2D NMR spectroscopy
✍ Scribed by Qin Li; Chunhui Yang; Ze-Mei Ge; Runtao Li; Yuxin Cui
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 97 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1808
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✦ Synopsis
Abstract
Compounds 1–7 form a novel group of dithiocarbamates, first synthesized from the reaction of a series of primary amines with carbon disulfide and 3‐bromo ethyl pyruvate in the presence of anhydrous potassium phosphate. Structure elucidation of this group of compounds was accomplished using extensive 1D and 2D NMR spectroscopic studies, including ^1^H, ^13^C, COSY, NOESY, HSQC, and gHMBC experiments. The distinction between the linear structures I, II and the cyclic structure III was made mainly on the basis of the analysis of the cross peak between H‐2 and H‐4a in the COSY spectra, in combination with the long‐range correlation between H‐2 and C‐4, 6 in the gHMBC spectra. Copyright © 2006 John Wiley & Sons, Ltd.
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