PubMed · 12757726
Solid-phase synthesis of a pepticinnamin E library.
Abstract
Pepticinnamin E is a naturally occurring bisubstrate inhibitor of farnesyltransferase. Based on the structure of the natural product, a compound library was synthesized by variation of eight structural parameters. Following three different routes, a total of 51 analogues was synthesized on the polymeric support in 6-11-step parallel syntheses. Overall yields ranged from 3 to 63%, and the compounds were obtained with >90% purity.
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Michael Thutewohl, Herbert Waldmann. 2003-06-12. Solid-phase synthesis of a pepticinnamin E library.. https://doi.org/10.1016/s0968-0896(03)00159-7
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