207982-19-2

Upstream product

• 207982-17-0 C₅₆H₆₄N₄O₂₂ 
• 207982-13-6 5-[5-Acetoxymethyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carbonyl]-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 207982-14-7 1-tert-Butoxycarbonyl-2,7-bis(2-methoxycarbonylethyl)-3,8-bis(methoxycarbonylmethyl)-9-(2,2,2-tribromoethoxycarbonyl)dipyrromethane 
• 207982-12-5 3-(2-Methoxycarbonyl-ethyl)-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-5-methyl-1H-pyrrole-2-carbonyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 207982-15-8 5-[5-Iodo-4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid 2,2,2-tribromo-ethyl ester 
• 207982-16-9 14-Benzyloxycarbonyl-2,8,13-tris(2-methoxycarbonylethyl)-4-[3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethyl-5-(2,2,2-tribromoethoxycarbonyl)pyrrol-2-ylmethyl]-3,7,12-tris(methoxycarbonylmethyl)-4,5-dihydrotripyrrin-1,10(15H,17H)-dione 
• 104705-81-9 5-Acetoxymethyl-4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid 2,2,2-tribromo-ethyl ester 
• 74839-05-7 5-Dimethylcarbamoyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 74855-24-6 5-Chlorocarbonyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 50622-64-5 benzyl 3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 75975-52-9 3-(2-Methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid tert-butyl ester 
• 207982-18-1 C₅₅H₆₃IN₄O₂₀ 

Relevant academic research and scientific papers

Biosynthesis of porphyrins and related macrocycles. Part 49. Exploration of synthetic routes to analogues of the spiro-intermediate for porphyrin biosynthesis

The proposed intermediacy of the spiro-pyrrolenine 1 for the biosynthesis of uroporphyrinogen III has focussed attention on its synthesis. Several different approaches to close analogues of this compound are explored, including (a) the synthesis of a dila