A novel and convenient route to L-homoserine lactones and L-phosphinothricin from L-aspartic acid
β Scribed by Michael G. Hoffmann; Hans-Joachim Zeiss
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 198 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
## Abstract A novel route with Lβascorbic acid as a single common starting material to asymmetric synthesis of all eight diastereomers of Lβhexoses is described. Assessment of this new approach is demonstrated by the expedient synthesis of Lβgalactopyranose and Lβtalopyranose derivatives. Key steps
In our investigation of the substrate specificity of 2-deoxy-n-ribose kinase isolated from Salmonella typhimurium, we required 2-deoxy-nribose (2-deoxy-L-erythro-pentose) (1) and 2-deoxy-D-xylose (2-deoxyn-threo-pentose) (2). Of the known methods for the preparation of these sugars (3, 4), the gly