Abstract
The title compound was produced diastereoselectively in racemic and optically active forms by employing the [2 + 2] cycloaddition reaction of an imine with benzyloxyketene followed by acidic alcoholysis of the formed 3,4-cis-disubstituted β-lactam with isopropanol.
| Original language | English |
|---|---|
| Pages (from-to) | 299-302 |
| Number of pages | 4 |
| Journal | Heterocycles |
| Volume | 30 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 1 1990 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Pharmacology
- Organic Chemistry
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Ito, Y., Kamijo, T., Harada, H., & Terashima, S. (1990). A novel synthesis of cyclohexylnorstatine isopropyl ester, the C-terminal component of a renin inhibitor. Heterocycles, 30(1), 299-302. https://doi.org/10.3987/com-89-s41