A new synthetic method of α-amino acids from α-methoxyurethanes
✍ Scribed by Tatsuya Shono; Yoshihiro Matsumura; Kenji Tsubata
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 97 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Reaction of a-methoxyurethanes with phenylisocyanide gave the corresponding amides of o-amino acid in reasonable yields.
📜 SIMILAR VOLUMES
## Abstract Diazotization of α‐amino acids in 48:52 (__w__/__w__) hydrogen fluoride/pyridine along with excess of potassium halide results in the corresponding α‐halocarboxylic acids in good to excellent yields __(Table 1__ and __2)__.
New Synthetic Routes to α-Amino Acids and γ-Oxygenated α-Amino Acids. Reductive Denitration and Oxidative Transformations of γ-Nitro-α-amino Acids. -In continuation of a recent work to synthesize γ-nitro α-amino acid derivatives, a novel approach to the title compounds such as (II), (III), (IV), (V