A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2017; you can also visit the original URL.
The file type is application/pdf.
Synthesis of chiral shiff base: Ferrocene-conjugates of amino acid esters
unpublished
Preserved Fulltext
Two novel chiral ferrocene-conjugates of amino acid esters were designed and prepared by condensation with formylFerrocene and enantiomerically pure amino acid esters. The products were characterized by melting point determination, rotation determination, IR, element analysis and 1 H-NMR. Esterification of amino acids using thionyl chloride results enantiomerically pure amino acid esters(L-Phenylalanine methyl ester and L-Leucine methylester).
fatcat:qo5hv7jomne7hcamou7ans2dby