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. Author manuscript; available in PMC: 2009 Dec 11.
Published in final edited form as: J Med Chem. 2008 Dec 11;51(23):7563–7573. doi: 10.1021/jm800997s

Table 2.

Yields and structural designs of class II 5″-modified neomycin derivatives

Compounds Carboxylic acids or amino acids Yield (%) Source of carboxylic acids
or amino acids
5a heptanoic acid (15) 88% Commercially available
5b palmitic acid (16)- 63% Commercially available
5c stearic acid (17)- 54% Commercially available
5d 2-phenyl-4-quinolinecarboxylic acid (18) 30% Commercially available
5e (S)-Z-4-amino-2-benzyloxybutyric acid (19) 90% Ref. 37
5f Z-Gly (20) 27% Commercially available
5g Z-l-Ala (21) 36% Commercially available
5h Z-l-Pro (22) 50% Commercially available
5i Z-l-Trp (23) 67% Commercially available
5j Z-l-Ser (24) 52% Commercially available
5k Z-l-Lys (25) 61% Commercially available
5l succinic anhydride (26) 85% Commercially available
5m Z-d-Ala (27) 69% Commercially available
5n Z-d-Ser (28) 57% Commercially available
5o Z-d-Pro (29) 53% Commercially available
5p Z-d-Lys (30) 25% Commercially available
5q Z-Gly-Gly (31) 42% Commercially available