Oxazolomycins: natural product lead structures for novel antibacterials by click fragment conjugation.
Conjugation of amide and lactam subunits by a 'Click' type approach provides access to structural mimics of the oxazolomycin series of natural products, some of which exhibit antibacterial activity.
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2010
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