The presence of the azetidin-2-one ring in several widely used families of antibiotics, which include the penicillins and carbapenems, has stimulated considerable activity directed at the stereocontrolled synthesis of b-lactams. [1] One of the most popular methods is the [22] cycloaddition reaction
Enantioselective Synthesis of 4-Unsubstituted 3-Alkoxy- and 3-Aminoazetidin-2-ones from Formaldehyde N,N-Dialkylhydrazones
✍ Scribed by Rosario Fernández; Ana Ferrete; José M. Lassaletta; José M. Llera; Angeles Monge
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 156 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0044-8249
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