78395-73-0

Upstream product

• 53603-63-7 1-methyl-2-phenyl-3-nitroso-1H-indole 
• 4993-86-6 2-phenyl-3,6-dinitroindole 
• 77-78-1 dimethyl sulfate 
• 67335-29-9 bis(1-methyl-2-phenyl-1H-indol-3-yl)methane 
• 78395-71-8 1-methyl-2-phenyl-3-nitro-1H-indole 
• 67335-20-0 3,3'-(phenylmethylene)bis(1-methyl-2-phenyl-1H-indole) 
• 62367-64-0 1-(1-methyl-2-phenyl-1H-indol-3-yl)ethan-1-one 
• 78395-78-5 1-methyl-2-phenyl-3-hydroxymethylindole 
• 4677-04-7 3-(phenyldiazenyl)-2-phenyl-1H-indole 
• 4771-06-6 2-phenyl-3-nitro-1H-indole 
• 17375-64-3 3-acetyl-2-phenylindole 
• 1757-72-8 1-methyl-2-phenyl-1H-indole-3-carbaldehyde 
• 56656-06-5 1-methyl-3-(methylthio)-2-phenyl-1H-indole 

Relevant academic research and scientific papers

ELECTRON-TRANSFER REACTIONS: REACTIONS OF INDOLES WITH NITROSONIUM ION. APPLICATION OF THE MARCUS THEORY. CRYSTAL STRUCTURES OF 1-METHYL-3,4-, 3,5- AND 3,6-DINITRO-2-PHENYLINDOLES

A series of 1-methyl-2-phenyl-3-substituted indoles, when reacted with nitrosonium tetrafluoroborate, formed mainly 3-nitro, 3,4-dinitro and 3,6-dinitro derivatives.Although Marcus theory agrees with the feasibility of an electron transfer (ET) between th

Electrophilic ipso-Substitutions. Part 1. Reaction of 3-Substituted Indoles with Nitronium and Nitrosonium Ions

3-Substituted indoles react with nitronium and nitrosonium ions to yield 3-nitroindole.In both cases the reaction was interpreted as an electrophilic ipso-substitution.The reaction mechanism is interpreted by hypothesizing the formation of a ?-complex-like intermediate, wich is some cases is preceded by an electron-transfer process.An order for the leaving abilities of the different electrofugal groups is discussed.