93454-33-2

Upstream product

• 93454-30-9 5,6,7,8-Tetrahydro-6-methyl-8-oxo-3H-pyrrolo<1,2-a>indole-9-carboxylic acid 
• 100-51-6 benzyl alcohol 
• 65481-20-1 Dimethyl 2(R)-acetoxy-2,3-dihydro-5-(3-carbomethoxy-2-methylpropyl)-1H-pyrrolizine-6,7-dicarboxylate 
• 65481-19-8 Dimethyl 2,3-dihydro-2(R)-hydroxy-5-(3-carbomethoxy-2-methylpropyl)-1H-pyrrolizine-6,7-dicarboxylate 
• 65481-22-3 Dimethyl 2,3,5,6,7,8-hexahydro-2(R)-hydroxy-6-methyl-8-oxo-1H-pyrrolo<1,2-a>indole-7,9-dicarboxylate 
• 79562-55-3 N-(4-Carbomethoxy-3-methylbutyroyl)-4-acetoxy-L-proline 
• 77198-71-1 2,3,5,6,7,8-Hexahydro-2(R)-<(methylsulfonyl)oxy>-6-methyl-8-oxo-1H-pyrrolo<1,2-a>indole-9-carboxylic acid 
• 93454-29-6 (S)-2-Hydroxy-6-methyl-8-oxo-2,3,5,6,7,8-hexahydro-1H-pyrrolo[1,2-a]indole-7,9-dicarboxylic acid 
• 77198-70-0 2,3,5,6,7,8-Hexahydro-2(R)-hydroxy-6-methyl-8-oxo-1H-pyrrolo<1,2-a>indole-9-carboxylic acid 
• 27151-65-1 3-methyl-1,5-pentanedioic acid monomethyl ester 

Downstream Products

• 93454-41-2 Benzyl cis-2,3,5,6,7,8-hexahydro-1-hydroxy-6-methyl-2-<(p-tolylsulfonyl)oxy>-8-oxo-1H-pyrrolo<1,2-a>indole-9-carboxylate 
• 93454-36-5 Benzyl cis-1,2-Dihydroxy-2,3,5,6,7,8-hexahydro-6-methyl-8-oxo-1H-pyrrolo<1,2-a>indole-9-carboxylate 

Relevant academic research and scientific papers

Total Synthesis of a Mitosene

The total synthesis of a mitosene (a chemical degradation product of mitomycin C) is described.The synthesis begins with hydroxyproline and uses a Huisgen pyrrole synthesis to form a pyrrolizidine system.The carbocyclic ring is made through Dieckmann cycl