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Synthetic Approaches toward Monocyclic 3‐Amino‐β‐lactams
| Content Provider | Semantic Scholar |
|---|---|
| Author | Deketelaere, Sari Nguyen, Tuyen Van Stevens, Christian V. D’hooghe, Matthias |
| Copyright Year | 2017 |
| Abstract | Due to the emerging resistance against classical β-lactam-based antibiotics, a growing number of bacterial infections has become harder to treat. This alarming tendency necessitates continued research on novel antibacterial agents. Many classes of β-lactam antibiotics are characterized by the presence of the 3-aminoazetidin-2-one core, which resembles the natural substrate of the target penicillin-binding proteins. In that respect, this Review summarizes the different synthetic pathways toward this key structure for the development of new antibacterial agents. The most extensively applied methods for 3-amino-β-lactam ring formation are discussed, in addition to a few less common strategies. Moreover, approaches to introduce the 3-amino substituent after ring formation are also covered. |
| Starting Page | 301 |
| Ending Page | 319 |
| Page Count | 19 |
| File Format | PDF HTM / HTML |
| DOI | 10.1002/open.201700051 |
| PubMed reference number | 28638759 |
| Journal | Medline |
| Volume Number | 6 |
| Alternate Webpage(s) | https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/14/47/OPEN-6-301.PMC5474669.pdf |
| Alternate Webpage(s) | https://doi.org/10.1002/open.201700051 |
| Journal | ChemistryOpen |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |