Synthesis of N-Succinyl-L,L-Diaminopimelic Acid Mimetics Via Selective Protection
作者:V. Vanek、J. Picha、M. Budesinsky、M. Sanda、J. Jiracek、R. Holz、J. Hlavacek
DOI:10.2174/092986610790780387
日期:2010.3.1
The search for potential inhibitors that target so far unexplored bacterial enzyme mono-N-succinyl-L,Ldiaminopimelic acid desuccinylase (DapE) has stimulated a development of methodology for quick and efficient preparation of mono-N-acylated 2,6-diaminopimelic acid (DAP) derivatives bearing the different carboxyl groups or lipophilic moieties on their amino group.
对尚未被广泛探索的细菌酶单-N-琥珀酰-L,L-二氨基庚二酸去琥珀酰酶(DapE)潜在抑制剂的搜索,促进了快速高效制备具有不同羧基或疏水基团的单-N-酰基-2,6-二氨基庚二酸(DAP)衍生物的方法发展。