The present invention is directed to carboxylic acid esters of deglucoteicoplanin, i.e. of the aglycon moiety of the antibiotic teicoplanin. The compounds of the invention are conveniently prepared either by deglucoteicoplanin or by any of the glycopeptides of the teicoplanin group, such as teicoplanin itself, one of its components, antibiotic L 17054 and antibiotic L 17046
Various dimeric derivatives of the glycopeptide antibiotic teicoplanin were prepared with the aim of...
The emergence of resistance among Gram-positive pathogens towards glycopeptide antibiotics has stimu...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to ester derivatives at the carboxylic function of the glycopeptid...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to a new antibiotic substance arbitrarily denominated antibiotic L...
The present invention is directed to a chemical process for preparing antibiotic L 17392 (deglucotei...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The aim of experiment is to synthesize a new teicoplanin pseudoaglycon derivative through a maleimid...
The title compds. [I; R = H, protecting group; Y = NR1X1(XX2)p(TX3)qW; R1 = H, alkyl; T, X = O, (sub...
Process for preparing antibiotic L, 17392 by catalytically hydrogenating a deglucoteicoplanin ester ...
The synthesis of the 16-membered cyclic DOEG ring system of teicoplanin, which forms the binding poc...
A series of lipophilic teicoplanin pseudoaglycon derivatives, including alkyl-, aryl-, calixarene- a...
Various dimeric derivatives of the glycopeptide antibiotic teicoplanin were prepared with the aim of...
The emergence of resistance among Gram-positive pathogens towards glycopeptide antibiotics has stimu...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to ester derivatives at the carboxylic function of the glycopeptid...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to a new antibiotic substance arbitrarily denominated antibiotic L...
The present invention is directed to a chemical process for preparing antibiotic L 17392 (deglucotei...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...
The aim of experiment is to synthesize a new teicoplanin pseudoaglycon derivative through a maleimid...
The title compds. [I; R = H, protecting group; Y = NR1X1(XX2)p(TX3)qW; R1 = H, alkyl; T, X = O, (sub...
Process for preparing antibiotic L, 17392 by catalytically hydrogenating a deglucoteicoplanin ester ...
The synthesis of the 16-membered cyclic DOEG ring system of teicoplanin, which forms the binding poc...
A series of lipophilic teicoplanin pseudoaglycon derivatives, including alkyl-, aryl-, calixarene- a...
Various dimeric derivatives of the glycopeptide antibiotic teicoplanin were prepared with the aim of...
The emergence of resistance among Gram-positive pathogens towards glycopeptide antibiotics has stimu...
The present invention is directed to the essentially pure preparation of an antibiotic substance arb...