Th.Ghanim, H., Oda.M.Yasser, , Abd-AL-Jabbbar.A.Mukhlis, (2011). Synthesis derivatives of 5, 6 -isopropylidene –N-{Methyl, Ethyl, Isopropyl, Isobutyl, Isopentyl, 2-phenylethyl}-gluconamide. , 0(42), 228-241.
Hasan. Th.Ghanim; Oda.M.Yasser; Abd-AL-Jabbbar.A.Mukhlis. "Synthesis derivatives of 5, 6 -isopropylidene –N-{Methyl, Ethyl, Isopropyl, Isobutyl, Isopentyl, 2-phenylethyl}-gluconamide". , 0, 42, 2011, 228-241.
Th.Ghanim, H., Oda.M.Yasser, , Abd-AL-Jabbbar.A.Mukhlis, (2011). 'Synthesis derivatives of 5, 6 -isopropylidene –N-{Methyl, Ethyl, Isopropyl, Isobutyl, Isopentyl, 2-phenylethyl}-gluconamide', , 0(42), pp. 228-241.
Th.Ghanim, H., Oda.M.Yasser, , Abd-AL-Jabbbar.A.Mukhlis, Synthesis derivatives of 5, 6 -isopropylidene –N-{Methyl, Ethyl, Isopropyl, Isobutyl, Isopentyl, 2-phenylethyl}-gluconamide. , 2011; 0(42): 228-241.

Synthesis derivatives of 5, 6 -isopropylidene –N-{Methyl, Ethyl, Isopropyl, Isobutyl, Isopentyl, 2-phenylethyl}-gluconamide

Iraqi National Journal Of Chemistry
Article 1, Volume 0, Issue 42, 2014, Pages 228-241
Authors
Hasan. Th.Ghanim; ;
Abstract
Abstract
Many new derivatives for L-ascorbic acid were prepared after closed the positions (2, 3, 5, and 6) in the L-ascorbic acid. Then its reaction with several amino acids (glycine, alanine, valine, leucine, phenylalanine). TLC, Elemental analysis, FTIR and H1.NMR spectroscopy, has characterized the synthesized compounds.
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