3560-45-0

Upstream product

• 93407-96-6 2-(((benzyloxy)carbonyl)amino)ethyl 4-methylbenzenesulfonate 
• 141-43-5 ethanolamine 
• 53844-02-3 benzyl N-(2-bromoethyl)carbamate 
• 134307-72-5 2-(((benzyloxy)carbonyl)amino)ethyl 1-methanesulfonate 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 111-41-1 2-(2-Aminoethylamino)ethanol 

Downstream Products

• 4533-15-7 N-Benzoyloxycarbonyl-N'-toluol-4-sulfonyl-N'-2-toluol-4-sulfonyloxyaethyl-aethylendiamin 
• 3560-46-1 N-Benzyloxycarbonyl-N'-2-iod-aethyl-N'-toluol-4-sulfonyl-aethylendiamin 
• 70889-93-9 N-(2-Benzyloxycarbonylaminoethyl)glycine 
• 911367-46-9 benzyl {(4S)-5-[(2-{[(benzyloxy)carbonyl]amino}ethyl)(2-hydroxyethyl)amino]-5-oxo-4-[(piperidin-3-ylcarbonyl)amino]pentyl}carbamate hydrochloride 
• 911367-45-8 tert-butyl 3-[(3S)-3-(3-{[(benzyloxy)carbonyl]amino}propyl)-5-(2-hydroxyethyl)-4,9-dioxo-11-phenyl-10-oxa-2,5,8-triazaundecan-1-oyl]piperidine-1-carboxylate 
• 911367-44-7 benzyl-{(4S)-4-amino-5-[(2-{[(benzyloxy)carbonyl]amino}ethyl)(2-hydroxyethyl)amino]-5-oxopentyl}carbamate hydrochloride 
• 1314801-19-8 (2-amino-ethyl)-(2-benzyloxycarbonylamino-ethyl)-carbamic acid tert-butyl ester 
• 1438898-21-5 C₂₅H₂₉N₃O₆ 
• 1438898-23-7 C₂₉H₄₀N₄O₁₀S 
• 1438898-22-6 C₂₃H₃₀N₄O₈S 
• 911367-57-2 benzyl {2-[{[(8S,11S,14S)-14-[(tert-butoxycarbonyl)amino]-11-{3-[(tert-butoxycarbonyl)amino]propyl}-5,17-dihydroxy-10,13-dioxo-9,12-diazatricyclo[14.3.1.1(2,6)]henicosa-1⁽²⁰⁾,2⁽²¹⁾,3,5,16,18-hexaen-8-yl]carbonyl}(2-hydroxyethyl)amino]ethyl}carbamate 
• 911367-43-6 benzyl-{2-[{(2S)-5-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]pentanoyl}-(2-hydroxyethyl)amino]ethyl}carbamate 

Relevant academic research and scientific papers

Synthesis of 12-membered macrocyclic templates and library analogs for PPI

We report novel syntheses of 12-membered macrocyclic templates and a library of 4000 macrocyclic analogs. The key macrocyclization step was performed at up to 100 g scale without resorting to syringe pumps, flow reactors or large volumes of solvent. An in

Preparation method N - (2 - aminoethyl) glycine derivative

The N - (2 - aminoethyl) glycine derivative product compound is obtained by taking hydroxyethyl ethylenediamine as a raw material, Cbz protecting the primary amine and then oxidizing the reaction, and N - (2 - aminoethyl) glycine derivative. To the prepar

ANTIBACTERIAL AMIDE MACROCYCLES VI

The invention concerns antibacterial amide macrocycles , methods for producing same, their use for treating and/or preventing diseases, as well as their use for producing drugs for treating and/or preventing diseases, in particular bacterial infections.