Preparation of amino acids from their hydrohalides via hexamethyldisilazane
โ Scribed by A. I. Yurtanov; Yu. A. Davidovich; S. V. Rogozhin
- Book ID
- 112437703
- Publisher
- Springer
- Year
- 1975
- Tongue
- English
- Weight
- 160 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Amino acid esters, formaldehyde and trinitromethane react readily in a Mannich type condensation to form N-trinitroethylamino acid esters in good yields. These products decompose slowly on standing but are stabilized by further nitration to the N-nitro-Ntrinitroethylamino esters. Hydrolysis of the e
Photooxidation of N-methoxy-2.4-disubstituted imidasoles, readily available by way of a three component cyclization followed by 0-allcylation, leads to stable acyl imines whhich react with various organometallics to afford cr,a-disubstituted amino acid m-amides in good yields. In an earlier communi