1393367-75-3

Upstream product

• 1393367-74-2 1-oxido-1-phenyl-1H-phosphindol-5-yl trifluoromethanesulfonate 
• 1393367-71-9 (E)-2-(5-(benzo[c]phenanthren-2-yl)oct-4-en-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1393367-81-1 5-hydroxy-1-phenyl-1H-phosphindole 1-oxide 

Downstream Products

• 1393478-57-3 10-phenyl-5,6-dipropyl-10H-naphtho[1',2':5,6]phenanthro[3,4-f]phosphindole 10-oxide 

Relevant academic research and scientific papers

1H-phosphindoles as structural units in the synthesis of chiral helicenes

Building helicenes: A photochemical cyclization approach affords helicenes in which the fused ring sequence ends with a phosphole unit (see scheme). The stereogenic phosphorus centers of the substrates control the screw sense of helical chirality. The terminal phosphole units undergo photochemical [2+2] annulations to give dimeric helical structures. Copyright