Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1370951 | Bioorganic & Medicinal Chemistry Letters | 2011 | 6 Pages |
Abstract
Imidazole analogs of the antibiotic natural product GE2270 A (1) were designed, synthesized, and evaluated for Gram positive bacteria growth inhibition. A recently reported, copper-mediated synthesis was exploited to prepare 4-thiazolyl imidazole analogs of 1. The synthesis described represents a structurally complex, natural product-based application of this recently reported synthetic methodology. In addition, the biological evaluation of the imidazole-based analogs further define the SAR of the 4-aminothiazolyl-based antibacterial template.
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Authors
Matthew J. LaMarche, Jennifer A. Leeds, JoAnne Dzink-Fox, Steve Mullin, Michael A. Patane, Elin M. Rann, Stacey Tiamfook,