One step synthesis of α-amido-β-lactams
✍ Scribed by Ajay K. Bose; H.P.S. Chawla; B. Dayal; M.S. Manhas
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 191 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
a-Sulfo-G-alanine was prepared by the oxidation of isocysteine (1) which in turn was prepared in low overall yield by multistep procedures, e.g. starting from an uracil derivative (2) or from S-alanine (3). Recently it was reported from this laboratory (4) that a-sulfa+-alanine is obtained in low yi
## Abstract Carbamoylketenes, generated in situ from substrates (I) or (IV) bearing an N‐aryl substituent, react with aldimines to give the title compounds in moderate yields.
Treatment of N,N-diallyl and N-alkyl, N-propargyl-p-ketoamides with NaH and then with N-iodosuccinimide led to the formation of iodomethyl-and iodomethylene-P-ketolactams.