159853-33-5

Upstream product

• 65874-43-3 9-(4-methoxyphenyl)-1H-phenalen-1-one 
• 1417620-53-1 ethyl 3-(2-(((trifluoromethyl)sulfonyl)oxy)naphthalene-1-yl)propanoate 
• 80515-84-0 ethyl 3-(2-hydroxynaphthalen-1-yl)propanoate 
• 1426148-37-9 4-(4-methoxyphenyl)-2,3-dihydro-1H-phenalen-1-one 
• 1417620-54-2 3-(2-(4-methoxyphenyl)naphthalen-1-yl)propanoic acid 
• 1426148-42-6 C₂₂H₂₂O₃ 
• 10441-53-9 3-(2-hydroxynaphthalen-1-yl)propanoic acid 
• 14233-73-9 3-(2-hydroxynaphthalen-1-yl)propanenitrile 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 548-39-0 Perinaphthenon 

Downstream Products

• 159853-36-8 2-hydroxy-4-(4-methoxyphenyl)-1H-phenalen-1-one 
• 149184-19-0 irenolone 
• 159853-35-7 3-(4-Methoxy-phenyl)-3b,4a-dihydro-4-oxa-cyclopropa[a]phenalen-5-one 

Relevant academic research and scientific papers

Phenalenone-type phytoalexins from Musa acuminata synthesis of 4-phenyl-penalenones

Two new 4-phenyl-phenalenone-type phytoalexins (2, 3) have been isolated from rhizomes of Musa acuminata infected with the fungus Fusarium oxysporum. The structures of the new phytoalexins were elucidated on the basis of spectroscopic evidence, chemical c

Improved synthesis of 4-phenylphenalenones: The case of isoanigorufone and structural analogs

2-Hydroxy-4-phenyl-1H-phenalen-1-one (isoanigorufone, 1), a phytoalexin exclusive of Musaceae, was synthesized starting from 3-(2-hydroxynaphthalen-1- yl)propanenitrile in nine steps in an overall yield of 10%. Hydrolysis of ethyl 3-(2-phenylnaphthalen-1-