917201-75-3

Upstream product

• 13030-09-6 1-benzyl L-glutamate 
• 866139-30-2 (S)-2-pyrrol-1-yl-pentanedioic acid 1-benzyl ester 
• 111-40-0 3-azapentane-1,5-diamine 

Downstream Products

• 1346772-41-5 (S)-4-(2-([2-((S)-4-benzyloxycarbonyl-4-(pyrrol-1-yl)-butyrylamino)-ethyl]-[(S)-4-((S)-2,6-bis(carbazol-9-yl)-hexyloxycarbonyl)-2-(carbazol-9-yl)-butyryl]-amino)-ethylcarbamoyl)-2-(pyrrol-1-yl)-butyric acid benzyl ester 
• 1346772-35-7 (S)-4-(2-[[2-((S)-4-benzyloxycarbonyl-4-(pyrrol-1-yl)-butyrylamino)-ethyl]-(4-(carbazol-9-yl)butyryl)-amino]-ethylcarbamoyl)-2-(pyrrol-1-yl)-butyric acid benzyl ester 
• 1346772-36-8 (S)-4-(2-[[2-((S)-4-benzyloxycarbonyl-4-(pyrrol-1-yl)-butyrylamino)-ethyl]-(2,6-bis(carbazol-9-yl)-hexanoyl)-amino]-ethylcarbamoyl)-2-(pyrrol-1-yl)-butyric acid benzyl ester 

Relevant academic research and scientific papers

Novel carboxylated pyrrole- and carbazole-based monomers. Synthesis and electro-oxidation features

(Chemical Equation Presented) Carboxylated pyrrole (Pyr, a index)- and carbazole (Cbz, b index)-containing monomers 6-7a/b and 9a/b have been readily synthesized from the monobenzyl ester of L-glutamic acid and triamine 2 using Clauson-Kaas and amide coup

Towards hybrid carbazole/pyrrole-based carboxylated monomers: Chemical synthesis, characterisation and electro-oxidation properties

Six novel hybrid carbazole (Cbz)-pyrrole (Pyr)-based carboxylated monomers were synthesised and unambiguously characterised using common spectroscopic tools. Clauson-Kaas, amide coupling, LAH (lithium aluminium hydride)-mediated reduction, esterification