86814-89-3

Upstream product

• 86814-83-7 (10R*,11R*)-10,11-Bis(hydroxymethyl)-4-phenyl-2,4,6-triazatricyclo<5.2.2.0^2,6>undec-8-en-3,5-dion 
• 6268-45-7 trans 1,2-Dicarbethoxy-cyclohexa-3,5-dien 
• 75529-48-5 trans-5,6-bis(hydroxymethyl)cyclohexa-1,3-diene 
• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 
• 86814-84-8 (10R*,11R*)-10,11-Bis<(methylsulfonyloxy)methyl>-4-phenyl-2,4,6-triazatricyclo<5.2.2.0^2,6>undec-8-en-3,5-dion 

Downstream Products

• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 
• 30168-21-9 1,2,3,4-Tetrahydro-N-phenyl-2,3-phthalazindicarboximid 
• 86814-91-7 1,2,3,4-Tetrahydro-N-methyl-2,3-phthalazindicarboximid 
• 86814-92-8 6-Methyl-14-phenyl-4,6,8,12,14,16-hexaazapentacyclo<9.5.2.0^2,10.0^4,8.0^12,16>octadeca-2(10),17-dien-5,7,13,15-tetron 

Relevant academic research and scientific papers

Attempts to Synthesize Derivatives of the 2,3-Diazabicycloocta-5,7-diene System

The 2,3-diazabicycloocta-5,7-diene derivatives 1a and b could neither be obtained by a photoaromatization reaction of 8 nor by an electrolytic oxidation of the dicarboxylic acids 13a,b.Cycloadditions to 21 lead to derivatives of the title system.At temperatures above -10 deg C these undergo a -cycloreversion to produce the tetrahydrophthalazines 22.The thermal transformation of 21 to 22 is rationalized on the basis of a chain mechanism.