852160-79-3

Upstream product

• 20303-31-5 benzyl 4-(2-methoxycarbonylethyl)-3,5-dimethylpyrrole-2-carboxylate 
• 54278-10-3 ethyl 5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrole-3-propanoate 
• 37789-64-3 4-(2-carboxyethyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 100-51-6 benzyl alcohol 

Downstream Products

• 871565-44-5 benzyl 3,5-dimethyl-4-[(S)-2-(1-(1-naphthyl)ethylcarbamoyl)ethyl]-1H-pyrrole-2-carboxylate 
• 871565-46-7 benzyl 3,5-dimethyl-4-[(R)-2-(1-(1-naphthyl)ethylcarbamoyl)ethyl]-1H-pyrrole-2-carboxylate 
• 871565-49-0 benzyl 4-[(S)-2-(benzyl-1-phenylethylcarbamoyl)ethyl]-3,5-dimethyl-1H-pyrrole-2-carboxylate 
• 884336-87-2 3-(2-tert-butoxycarbonylethyl)-4-methyl-1H-pyrrole-2,5-dicarboxylic acid 5-benzyl ester 
• 884336-91-8 4-(2-tert-butoxycarbonyl-ethyl)-5-dichloromethyl-3-methyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 884336-92-9 4-(2-tert-butoxycarbonyl-ethyl)-5-formyl-3-methyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 884336-86-1 4-(2-tert-butoxycarboxnylethyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 852160-81-7 benzyl 3,5-dimethyl-4-[(R)-2-(1-phenyl-ethylcarbamoyl)-ethyl]-1H-pyrrole-2-carboxylate 
• 871565-51-4 benzyl 4-[(R)-2-(benzyl-1-phenylethylcarbamoyl)ethyl]-3,5-dimethyl-1H-pyrrole-2-carboxylate 

Relevant academic research and scientific papers

Asymmetric synthesis of mono- and dinuclear bis(dipyrrinato) complexes

(Chemical Equation Presented) The diastereoselective syntheses of Zn(II) bis(dipyrrinato) helicates is reported, involving ligands templated by the incorporation of homochiral binol within the linker joining the two dipyrrinato units. The most diastereose

Synthesis of orthogonally protected pyrrole tricarboxylic acid derivatives: Versatile building blocks for pyrrole-containing compounds

The large-scale synthesis of three new orthogonally protected pyrrole tricarboxylates 1-3 is described. Using different cleavage conditions, each of the three carboxylates can be set free selectively without affecting the others, making these pyrrole derivatives versatile synthetic building blocks for a wide range of applications in natural product or supramolecular chemistry. Georg Thieme Verlag Stuttgart.

Stereochemically stable double-helicate dinuclear complexes of bis(dipyrromethene)s: A chiroptical study

Helical zinc(II) complexes of bis(dipyrromethene)s bearing homochiral amide substituents were synthesized. Analysis of the products by chiral HPLC showed two diastereomeric major products and showed that dipyrromethene double-nuclear helicates are stereoc