3.8 Article

Solution- and solid-phase syntheses of substituted guanidinocarboxylic acids

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JOURNAL OF COMBINATORIAL CHEMISTRY
卷 2, 期 3, 页码 276-281

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AMER CHEMICAL SOC
DOI: 10.1021/cc990084b

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  1. NIDA NIH HHS [DA09358] Funding Source: Medline
  2. NIGMS NIH HHS [GM46535] Funding Source: Medline

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A library of guanidine-based compounds was produced to mimic the lead compound 1, which is a substance known to have intensely sweet-taste characteristics. Libraries of guanidinocarboxylic acids were therefore prepared via two synthetic methods. The solid-phase method involving trapping of solution-phase carbodiimides by supported amines was used to produce N,N'-dialkyl derivatives (Scheme I). The second solid-phase method, featuring supported carbodiimides and solution-phase amines (Scheme 2), was devised to prepare N,N'-disubstituted and N,N',N'-trisubstituted guanidinocarboxylic acids. A small collection of guanadinoacetic acid dimers mid trimers was also prepared, but this time via a solution-phase coupling of carbodiimides to a polyamine linker.

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