111807-55-7

Upstream product

• 77929-43-2 3-(2-Methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-5-trichloromethyl-1H-pyrrole-2-carboxylic acid benzyl ester 
• 50622-64-5 benzyl 3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethyl-5-methylpyrrole-2-carboxylate 
• 115-20-8 1,1,1-trichloroethanol 
• 72423-57-5 5-benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3methoxycarbonylmethylpyrrole-2-carboxylic acid 

Downstream Products

• 55305-15-2 3,3'-bis-(2-methoxycarbonyl-ethyl)-4,4'-bis-methoxycarbonylmethyl-1H,1'H-5,5'-methanediyl-bis-pyrrole-2-carboxylic acid dibenzyl ester 
• 206861-06-5 C₃₄H₃₇Cl₃N₂O₁₂ 

Relevant academic research and scientific papers

New method for the synthesis of pyrromethanes

Coupling reaction of 2-mercaptobenzothiazolylmethylpyrrole with α-free pyrrole in the presence of silver(I) triflate proceeds smoothly at room temperature to give a pyrromethane in excellent yield. The azafulvenium ion, an active form that reacts with α-f

2-Mercaptobenzothiazolylmethylpyrrole as a new means for the synthesis of pyrromethanes under neutral conditions

The coupling reaction of 2-mercaptobenzothiazolylmethylpyrrole 4b with α-free pyrrole 2b in the presence of silver (I) triflate proceeds smoothly at room temperature to give pyrromethane 1b in excellent yield. 4b reacts rapidly with pyrromethane 1b under

Synthetic and Biosynthetic Studies of Porphyrins. Part 9. Synthesis of Isocoproporphyrin, Dehydroisocoproporphyrin, and De-ethylisocopropophyrin

The title compounds, which were extracted by patients suffering from porphyria cutanea tarda or rats poisoned with hexachlorobenzene have been synthesized by the b-oxobilane route.Isocoproporphyrin tetramethyl ester (7a) were prepared from pyrromethanes c