210428-12-9

Upstream product

• 132388-69-3 Boc-L-Gln(Trt)-OH 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 74-88-4 methyl iodide 

Downstream Products

• 199005-57-7 Boc-Gln(Trt)-H 
• 817208-62-1 [3-tert-butoxycarbonylamino-2-oxo-5-(tritylcarbamoyl)pentyl]phosphonic acid dimethyl ester 
• 817208-65-4 5-tert-butoxycarbonylamino-2-[3-(tert-butyldimethylsilanyloxy)propyl]-4-oxo-7-(tritylcarbamoyl)hept-2-enoic acid methyl ester 
• 210428-15-2 (E)-(S)-3-tert-Butoxycarbonylamino-5-(trityl-carbamoyl)-pent-1-ene-1-sulfonic acid ethyl ester 
• 210428-17-4 (E)-(S)-3-tert-Butoxycarbonylamino-5-(trityl-carbamoyl)-pent-1-ene-1-sulfonic acid methyl ester 
• 210428-22-1 {(E)-(S)-3-Chlorosulfonyl-1-[2-(trityl-carbamoyl)-ethyl]-allyl}-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of β-ketophosphonate analogs of glutamyl and glutaminyl adenylate, and selective inhibition of the corresponding bacterial aminoacyl-tRNA synthetases

The aminoacyl-β-ketophosphonate-adenosines (aa-KPA) are stable analogs of the aminoacyl adenylates, which are high-energy intermediates in the formation of aminoacyl-tRNA catalyzed by aminoacyl-tRNA synthetases (aaRS). We have synthesized glutamyl-β-ketop

Synthesis of a tripeptide derivative containing the Gln-Arg hydroxyethylene dipeptide isostere

(Chemical Equation Presented) The protected hydroxyethylene dipeptide isostere of Gln-Arg and the tripeptide derivative 1 were synthesized as components of potential peptidase inhibitors.