123267-31-2

Upstream product

• 123267-30-1 4,5-Bis-benzenesulfonyloxy-phthalic acid dimethyl ester 
• 98-09-9 benzenesulfonyl chloride 
• 66323-03-3 4,5-bis(hydroxy)phthalic acid dimethyl ester 

Downstream Products

• 123267-36-7 8-((phenylsulfonyl)oxy)-7-methoxy-2,3,11,11a-tetrahydropyrrolo<1,2-b><2>benzazepine-5,10(1H)-dione 
• 123267-37-8 Benzenesulfonic acid 8-methoxy-5,10-dioxo-2,3,5,10,11,11a-hexahydro-1H-benzo[e]pyrrolo[1,2-a]azepin-7-yl ester 
• 123267-35-6 4-((phenylsulfonyl)oxy)-5-methoxy-N-(4-pentenyl)-phthalimide 
• 123267-33-4 4-((phenylsulfonyl)oxy)-5-methoxyphthalic acid 
• 123267-34-5 4-((phenylsulfonyl)oxy)-5-methoxyphthalimide 
• 123267-32-3 dimethyl 4-((phenylsulfonyl)oxy)-5-methoxyphthalate 

Relevant academic research and scientific papers

Photochemical Approach to the Synthesis of the Pyrrolobenzodiazepine Antibiotics

The total syntheses of the pyrrolobenzodiazepine antitumor antibiotics prothracarcin and DC-81 were realized using, as a key step, the photochemical ring expansion of the appropriately substituted N-pentenylphthalimide to afford the corresponding pyrrolobenzazepinedione.Conversion of the photoproduct into the antibiotic skeleton was effected by transformation of the benzylic ketone into a carbinolamine via a Curtius rearrangement sequence.