Reaction of 2-amino-3-phenylcarbamoylazirine with acid chlorides
✍ Scribed by A. V. Eremeev; I. P. Piskunova; R. S. Él'kinson
- Book ID
- 112349030
- Publisher
- Springer US
- Year
- 1984
- Tongue
- English
- Weight
- 63 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Reaction of 2-amino-5-R-phenyl-!,3,4-thiadizoles with unsaturated acids and acid chlorides in the presence of trimethylamine takes place exclusively at the amino group to form the 2-carboxyalkyl-and 2-acylamino-derivatives, respectively. 2-Amino-l,3,4-thiadiazoles, including their acyl derivatives,
Reactions of N-protected amino acid chlorides with carbonyl compounds in the presence of SmI2 were investigated. Decarbonylation followed by a cross coupling between amino moiety and aldehyde or ketone is observed. By the use of FMOC derivatives, N-protected amino alcohols were isolated in moderate