Penem synthesis through C3-N ring closure of a .beta.-lactam precursor
✍ Scribed by Wasserman, Harry H.; Han, William T.
- Book ID
- 125834635
- Publisher
- American Chemical Society
- Year
- 1985
- Tongue
- English
- Weight
- 400 KB
- Volume
- 107
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Reported here is the synthesis and characterization of the indenopyrrolocarbazole ring system utilizing a Diels‐Alder reaction with 2‐indenylindole and maleimide. Clemmensen reduction of imide **10** furnished the 5‐oxo (**16**) and 7‐oxo (**17**) lactam regioisomers. A new regiospecifi
## Abstract In this contribution, aminocyclobutanes, as well as eight‐membered enamide rings, have been made from __N__‐vinyl β‐lactams. The eight‐membered products have been formed by a [3,3]‐sigmatropic rearrangement, whereas the aminocyclobutanes have been derived from a domino [3,3]‐rearrangeme