57907-68-3

Upstream product

• 75630-44-3 1-Iodomethyl-3-methoxycarbonylmethyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid methyl ester 
• 50622-72-5 4-iodo-3-methoxycarbonylmethyl-5-methyl-pyrrole-2-carboxylic acid methyl ester 
• 50622-73-6 methyl 3-<(methoxycarbonyl)methyl>-5-methylpyrrole-2-carboxylate 
• 124-41-4 sodium methylate 
• 62562-72-5 benzyl 3-(benzyloxycarbonylmethyl)-4,5-dimethylpyrrole-2-carboxylate 
• 75630-45-4 methyl 4,5-dimethyl-3-(methoxycarbonylmethyl)pyrrole-2-carboxylate 

Downstream Products

• 129689-57-2 dibenzyl 3-ethyl-4'-methoxycarbonylmethyl-4,3'-dimethyl-2,2'-dipyrrylmethane-5,5'-dicarboxylate 
• 75747-97-6 dibenzyl 4,4'-bis(2-acetoxyethyl)-3,3'-dimethylpyrromethane-5,5'-dicarboxylate 
• 75630-47-6 dibenzyl 3,3'-dimethyl-4,4'-bis(methoxycarbonylmethyl)pyrromethane-5,5'-dicarboxylate 
• 75630-48-7 dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate 
• 75630-46-5 benzyl 5-acetoxymethyl-3-(methoxycarbonylmethyl)-4-methylpyrrole-2-carboxylate 

Relevant academic research and scientific papers

Biosynthesis of Porphyrins and Related Macrocycles. Part 13. Structure of the Protoporphyrin Isomer derived from Coproporphyrinogen lV by the Action of Beef-Liver Coproporphyrinogenase: Synthesis of Protoporphyrin Xlll

Coproporphyrinogen lV (8) is synthesised and is oxidatively decarboxylated by coproporphyrinogenase from beef-liver to produce, after aromatisation, a porphyrin proved to be protoporphyrin Xlll (11) by spectroscopy and by unambiquous synthesis; the synthesis route is described.A monovinylporphyrin, derived from an intermediate for the conversion (8) -> (11), is also isolated.The importance of these results for earlier biosynthetic studies with pyrromethanes is discussed.