The present invention relates to novel depsipeptide compounds. The invention also relates to pharmaceutical compositions of these compounds and methods of using these compounds as antibacterial compounds. The invention also relates to methods of producing these novel depsipeptide compounds and intermediates used in producing these compounds.
-
Page/Page column 375
(2010/11/30)
Synthesis of (R)-4-oxo-5-phosphononorvaline, an N-methyl-D-aspartic acid receptor selective β-keto phosphonate
(R)-4-Oxo-5-phosphononorvaline (1), a selective NMDA glutamate site antagonist, has been synthesized in four steps (overall yield = 31%) from (R)-aspartic acid, without racemization.
Rudisill,Whitten
p. 851 - 854
(2007/10/02)
Synthesis and rearrangement of homoserine derivatives
-
Baldwin,North,Flinn
p. 637 - 642
(2007/10/02)
More Articles about upstream products of 116393-73-8