✦ LIBER ✦
Chemical properties of the natural neurotoxin of Lathyrus sativus 3-N-oxalyl-2,3-diamino-propanoic acid (β-ODAP), its nontoxic 2-N-oxalyl isomer, and its hydrolysis product 2,3-diamino-propanoic acid (DAPRO) by 1H- and 13C-NMR spectroscopy
✍ Scribed by Dr. André De Bruyn; Dirk Van Haver; Fernand Lambein; Berhanu M. Abegaz
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 760 KB
- Volume
- 1
- Category
- Article
- ISSN
- 1056-9014
No coin nor oath required. For personal study only.
✦ Synopsis
The 'H and 13C NMR data of DAPRO, a-and p-ODAP were measured at varying pH values and the physical relevance of these data was studied. As a potential way to detoxify the neurotoxin p-ODAP, its isomerization was studied at room temperature and at 60°C. An unknown hydrolysate is identified as