95305-17-2

Upstream product

• 95305-10-5 5-(3-ethyl-4-methyl-5-t-butoxycarbonylpyrrol-2-ylmethyl)-4,4-dimethylpyrrolidin-2-thione 
• 95305-16-1 tert-Butyl 5-benzyloxycarbonyl(bromo)methyl-4-ethyl-3-methylpyrrole-2-carboxylate 
• 924-50-5 Methyl 3,3-dimethylacrylate 
• 79264-56-5 t-butyl 5-(4-methoxycarbonyl-3,3-dimethyl-2-nitrobutyl)-4-ethyl-3-methylpyrrole-2-carboxylate 
• 95305-09-2 5-(3-ethyl-4-methyl-5-t-butoxycarbonylpyrrol-2-ylmethyl)-1-hydroxy-4,4-dimethylpyrrolidin-2-one 
• 95305-11-6 tert-Butyl 5-benzyloxycarbonylmethyl-4-ethyl-3-methylpyrrole-2-carboxylate 
• 79264-57-6 5-(3-ethyl-4-methyl-5-t-butoxycarbonylpyrrol-2-ylmethyl)-4,4-dimethylpyrrolidin-2-one 
• 79264-55-4 t-butyl 4-ethyl-3-methyl-5-(2-nitroethyl)pyrrole-2-carboxylate 
• 95305-12-7 5-Chlorocarbonyl-4-ethyl-3-methyl-1H-pyrrole-2-carboxylic acid tert-butyl ester 
• 31897-11-7 5-tert-Butoxycarbonyl-3-ethyl-4-methylpyrrole-2-carboxylic Acid 

Downstream Products

• 95305-18-3 di-t-butyl 5-benzyloxycarbonyl-3,12-diethyl-2,8,8,13-tetramethyl-7,8,9,10,16,17-hexahydrotripyrrin-1,14-dicarboxylate 

Relevant academic research and scientific papers

Synthetic Studies Relevant to Biosynthetic Research on Vitamin B12. Part 2. Syntheses of C-Methylated Chlorins Via Lactams

C-Metylyted chlorins have been synthesised by two approaches.For one, ring-B and ring-C of the final chlorin were built sequentially onto a thiolactam system which acted as the A-D component.The preferred alternative method involved joining together a lac