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[摘要]：The design and synthesis of small molecule alpha-helix mimetics has been a productive field over the past decade. These compounds have performed well in a variety of biological, systems as functional disruptors of alpha-helix-mediated protein protein interactions. In our studies we have continued to develop novel, more biologically compatible scaffolds, which are often easier to assemble and capable of mimicking longer and/or more diverse helices. To this end, we have constructed a new series of i, i+4, i+7 alpha-helix mimics based on the enaminone scaffold. These molecules represent a step forward in the pursuit of idealized monofacial alpha-helix mimetics. |
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