75630-46-5

Upstream product

• 50622-73-6 methyl 3-<(methoxycarbonyl)methyl>-5-methylpyrrole-2-carboxylate 
• 62562-72-5 benzyl 3-(benzyloxycarbonylmethyl)-4,5-dimethylpyrrole-2-carboxylate 
• 75630-45-4 methyl 4,5-dimethyl-3-(methoxycarbonylmethyl)pyrrole-2-carboxylate 
• 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 
• 546-67-8 lead(IV) tetraacetate 
• 57907-68-3 benzyl 3-(methoxycarbonylmethyl)-4,5-dimethylpyrrole-2-carboxylate 

Downstream Products

• 129689-57-2 dibenzyl 3-ethyl-4'-methoxycarbonylmethyl-4,3'-dimethyl-2,2'-dipyrrylmethane-5,5'-dicarboxylate 
• 108802-20-6 C₂₉H₃₆N₂O₆ 
• 75630-48-7 dibenzyl 3,3'-bismethyl-4,4'-bis-(2-hydroxyethyl)pyrromethane-5,5'-dicarboxylate 
• 75747-97-6 dibenzyl 4,4'-bis(2-acetoxyethyl)-3,3'-dimethylpyrromethane-5,5'-dicarboxylate 
• 87377-78-4 dibenzyl 3,4'-bis(2-hydroxyethyl)-4,3'-dimethylpyrromethane-5,5'-di-carboxylate 
• 87377-79-5 dibenzyl 3,4'-bis(2-acetoxyethyl)-4,3'-dimethylpyrromethane-5,5'-dicarboxylate 
• 26280-00-2 biliverdin IX_γ dimethyl ester 
• 79760-31-9 γ-benzoyloxy-2,4-di(2-chloroethyl)-6,7-di(2-methoxycarbonylethyl)-1,3,5,8-tetramethylporphyrin 
• 79760-30-8 Benzoic acid (5E,10Z,14Z,19Z)-13,18-bis-(2-hydroxy-ethyl)-3,7-bis-(2-methoxycarbonyl-ethyl)-2,8,12,17-tetramethyl-porphyrin-5-yl ester 
• 79760-29-5 2,4-bis(2-acetoxyethyl)-γ-benzoyloxy-6,7-bis(2-methoxycarbonylethyl)-1,3,5,8-tetramethylporphyrin 
• 75630-47-6 dibenzyl 3,3'-dimethyl-4,4'-bis(methoxycarbonylmethyl)pyrromethane-5,5'-dicarboxylate 
• 87377-77-3 dibenzyl 3-ethoxycarbonylmethyl-4'-methoxycarbonylmethyl-4,3'-dimethylpyrromethane-5,5'-dicarboxylate 
• 108785-12-2 C₂₉H₃₆N₂O₆ 

Relevant academic research and scientific papers

The Chemistry of Pyrrolic Compounds. LXV Intramolecular Cyclization of Porphyrins with Acetic Acid Chains: Hydroxy Derivatives of Deoxophylloerythroaetioporphyrin (DPEP)

The intramolecular cyclization of porphyrins substituted with an acetic acid side chain has been studied under a range of conditions but the yield of product bearing a fused five-membered ketonic ring system was disappointingly low.Deoxophylloerythroaetio

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.