62562-77-0

Upstream product

• 87308-15-4 benzyl 3-<<(benzyloxy)carbonyl>methyl>-4-formyl-5-methylpyrrole-2-carboxylate 
• 62562-74-7 benzyl 4-<<(benzyloxy)carbonyl>methyl>-2-methylpyrrole-5-carboxylate 
• 53700-88-2 Ethyl 3-(ethoxycarbonyl)methyl-5-methylpyrrole-2-carboxylate 
• 62562-76-9 benzyl 3-(2-hydroxyethyl)-4,5-dimethylpyrrole-2-carboxylate 

Downstream Products

• 92735-24-5 benzyl 3-(2-chloroethyl)-5-formyl-4-methylpyrrole-2-carboxylate 
• 89909-57-9 tert-butyl 2-<(benzyloxy)carbonyl>-3-(2-chloroethyl)-4-methylpyrrole-5-carboxylate 
• 104834-46-0 2-<(benzyloxy)carbonyl>-3-(2-chloroethyl)-4-methylpyrrole-5-carboxylic acid 
• 104834-45-9 benzyl 3-(2-chloroethyl)-4-methylpyrrole-2-carboxylate 
• 104834-44-8 benzyl 3-(2-chloroethyl)-5-iodo-4-methylpyrrole-2-carboxylate 
• 135363-70-1 Dibenzyl 3,4'-Bis(2-chloroethyl)-1,3',4-trimethyldipyrromethane-5,5'-dicarboxylate 
• 5522-66-7 protoporphyrin IX dimethyl ester 

Relevant academic research and scientific papers

Methyl Deuteration Reactions in Vinylporphyrins: Protoporphyrins IX, III, and XIII

Base-catalyzed deuteration of the methyl groups in protoporphyrin IX dimethyl ester (1) proceeds with differential deuteration; rate of deuteration, as measured by NMR spectroscopy of reaction products, follows the order 3-Me > 1-Me >5-Me >8-Me.A simple q

Neighboring Group Participation in the Pyrrole Series

With use of proton and carbon-13 NMR spectroscopy of deuterium- and carbon-13-labeled substrates, the transformation of certain (2-hydroxyethyl)pyrroles (4, 18, 21) into the corresponding (2-haloethyl)pyrroles (using thionyl chloride/pyridine or triphenyl