Practical synthesis of optically active α-hydrazino acids from α-amino acids
✍ Scribed by Joëlle Viret; Jacqueline Gabard; André Collet
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 290 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Simple amino acids (1) can be converted in fair to good yield into hydrazino acids (3) of like configuration by using KOCI instead of NaOCl to promote the Shestakov rearrangement of the intermediate hydantoic acids (2). It was shown fifteen years ago by Karady et al.,' and later by Custafsson,' that simple amino acids (1) can
📜 SIMILAR VOLUMES
## Abstract The reaction of O‐menthyl phenylphosphonite **__1__** with aromatic aldehydes in the presence of Me~3~SiCl provided the O‐menthyl α‐hydroxyphosphinates **__2__**. Acidic hydrolysis of **__2__** gave the corresponding α‐hydroxyphosphinic acids **__3__**. The (+)‐enantiomer of **__3a__**