1319735-08-4

Upstream product

• 5159-41-1 2-iodobenzyl alcohol 
• 627-19-0 1-Pentyne 
• 120-72-9 indole 
• 1319735-04-0 2-pent-1-ynylbenzyl bromide 

Downstream Products

• 1319735-30-2 11-[1-o-tolylbut-(Z)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 
• 1319735-34-6 11-[1-(3-trifluoromethylphenyl)but-(Z)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 
• 1319735-29-9 11-[1-p-tolylbut-(Z)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 
• 1319735-55-1 3-deutero-1-(2-pent-1-ynylbenzyl)-1H-indole 
• 1319735-27-7 11-[1-phenylbut-(Z)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 
• 1319735-28-8 11-[1-phenylbut-(E)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 
• 103-26-4 methyl cinnamate 
• 1319735-32-4 11-[1-(4-bromophenyl)but-(Z)-ylidene]-6,11-dihydroindolo[1,2-b]isoquinoline 

Relevant academic research and scientific papers

Tandem indole C-H alkenylation/arylation for tetra-substituted alkene synthesis

Alkynyl indoles undergo a novel sequence of Pd-catalysed indole C-H activation/alkyne carbopalladation/arylation, with diaryliodonium salts providing the aryl components. An array of functionalised indole alkenes have been prepared in good to excellent yield, with the reaction being selective for the Z-alkene.