
%0 Journal Article
%A Black, DSC 
%A Brown, RFC 
%A Wade, AM 
%T Synthetic studies related to mycobactins. II. Formation of mycobactin hydroxamic acid units by malonic ester synthesis
%J Australian Journal of Chemistry
%D 1972/10/01
%V 25
%N 10
%P 2155-2166
%K 
%R https://doi.org/10.1071/CH9722155
%U https://www.publish.csiro.au/paper/CH9722155 
%X 6-(N-Hydroxy)lysine dihydrochloride and some related compounds have been synthesized by a reaction sequence involving the alkylation of sodium diethyl-phthalimidomalonate by 1,4-dibromobutane to form diethyl 5-bromo-1-phthalimido-pentane-1,l-dicarboxylate. During the transformation of this bromo compound to the corresponding nitro compound, cyclization to diethyl l-(2'-carboxybenzoyl)piperidine-2,2-dicarboxylate occurred. 
