37945-51-0

Upstream product

• 37945-46-3 1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indol-5-one 
• 3744-82-9 3,4-dihydrobenzo[cd]indol-5(1H)-one 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 81206-38-4 4-azido-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indol-5-one 
• 41455-40-7 4-amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 41455-46-3 4-[N-(methoxycarbonyl)-N-propargyl]amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 41455-42-9 4-(N-methoxycarbonyl)amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 744970-29-4 4-[N-(methyl)-N-acetonyl]amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 41455-47-4 4-[N-(methoxycarbonyl)-N-acetonyl]amino-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indol-5-one 
• 83402-24-8 5-ethylenedioxy-4-formamido-1,3,4,5-tetrahydro-1-(p-tolylsulphonyl)benzindole 
• 41455-73-6 4-(N-acetyl)amino-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indol-5-one 
• 849413-44-1 4-azido-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 849413-49-6 4-N-(methyl)amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 849413-55-4 4-N-(methyl)amino-5,5-diethoxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 849413-52-1 4-azido-5,5-diethoxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 849413-53-2 4-amino-5,5-diethoxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 
• 849413-54-3 4-N-(formyl)amino-5,5-diethoxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]indole 

Relevant academic research and scientific papers

Chemistry of indoles carrying a basic function. Part IX. Unexpected cyclizations of diketones derived from Uhle's ketone

Starting from a tricyclic diketone (14) obtained by Bowman's method, a tetracyclic oxonaphthalene derivative (17) has been prepared through intramolecular aldol condensation followed by indole → naphthalene isomerization. An unexpected formation of a lact

Morpholine derivatives and their use

A compound represented by the formula STR1 wherein X is hydrogen or a substituent; R1 is an optionally substituted hydrocarbon residue; R2 and R3 are respectively hydrogen or a substituent; and ----- shows a single bond or