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Synthesis of biologically active 3 bromo-1: 8-naphthalylamino acid dipeptide derivatives
Egyptian Journal of Chemistry. 1982; 25 (5): 445-51
in En | IMEMR | ID: emr-1817
Responsible library: EMRO
Synthesis of a series of 3-bromo-l: 8-naphthalylamino acids [II-VIII] and their corresponding methyl esters [IX-XIII]is described. Coupling of 3-bromo-l: 8-naphthalylamino acids with amino acid methyl ester hydrochlorides [or urea or 2-amino-pyridine] in dioxane-DMF-Et, N medium using DCC method, furnishes the desired 3-bromo-l: 8-naphthalyldipeptides[XIV-XXVIII]. All 3-bromo-l-8-naphthalyl derivatives of L-valine, L-leucine, DL-phenylalamtie and [S-alanine and their methyl esters and most dipeptide derivatives were found to possess high antimicrobial activities towards different microorganisms
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Index: IMEMR Main subject: Amino Acids / Naphthalenes Language: En Journal: Egypt. J. Chem. Year: 1982
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Index: IMEMR Main subject: Amino Acids / Naphthalenes Language: En Journal: Egypt. J. Chem. Year: 1982