From aziridines to carbapenems via a novel β-lactam ring closure
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Enantioselective Syntheses of Carbapenem Antibiotics
2. An aziridine route to chiral β-lactams a novel entry to (+)-thienamycin
3. The first practical method for asymmetric epoxidation
4. The e.e. of epoxy alcohol 3 was estimated to at least 97% by R NMB spectroscopy on the corresponding acetate in the presence of Eu(tfc)3, after a suitable control experiment on the racemic acetate.
5. A new aziridine synthesis from 2-azido alcohols and tertiary phosphines. Preparation of phenanthrene 9,10-imine
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