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Solution- and solid-phase syntheses of substituted guanidinocarboxylic acids.

Authors :
Chen J
Pattarawarapan M
Zhang AJ
Burgess K
Source :
Journal of combinatorial chemistry [J Comb Chem] 2000 May-Jun; Vol. 2 (3), pp. 276-81.
Publication Year :
2000

Abstract

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 1). 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 and trimers was also prepared, but this time via a solution-phase coupling of carbodiimides to a polyamine linker.

Details

Language :
English
ISSN :
1520-4766
Volume :
2
Issue :
3
Database :
MEDLINE
Journal :
Journal of combinatorial chemistry
Publication Type :
Academic Journal
Accession number :
10827936
Full Text :
https://doi.org/10.1021/cc990084b