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
Asymmetric Synthesis of trans-3-Amino-4-alkylazetidin-2-ones from Chiral N,N-Dialkylhydrazones.
β Scribed by Elena Diez; Rosario Fernandez; Eugenia Marques-Lopez; Eloisa Martin-Zamora; Jose M. Lassaletta
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 21 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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