150267-59-7

Upstream product

• 150267-58-6 2-Allyl-4-methoxy-6-isopropylphenol 
• 77-78-1 dimethyl sulfate 
• 26307-50-6 4-bromo-2-isopropyl-phenol 
• 153341-13-0 Allyl 4-bromo-2-isopropylphenyl ether 
• 150267-57-5 Allyl 4-methoxy-2-isopropylphenyl ether 

Downstream Products

• 155191-00-7 4-(2,5-Dimethoxy-3-isopropylphenyl)butyraldehyde 
• 150267-60-0 3-(3-Isopropyl-2,5-dimethoxy-phenyl)-propan-1-ol 
• 142950-86-5 triptoquinone A 
• 137758-96-4 (+/-)-triptoquinone A 
• 155191-01-8 4-(2,5-Dimethoxy-3-isopropylphenyl)butyric acid 
• 153341-07-2 2-Hydroxy-5,8-dimethoxy-1,4a-dimethyl-7-isopropyl-2-(1-methoxy-1-(diphenylphosphoryl)methyl)-2,3,4,4a,9,10-hexahydrophenanthrene 
• 155321-08-7 (E)-9-(3-Isopropyl-2,5-dimethoxy-phenyl)-2,6-dimethyl-3-oxo-non-6-enoic acid ethyl ester 
• 155191-78-9 (E)-5-(3-Isopropyl-2,5-dimethoxy-phenyl)-2-methyl-pent-2-enoic acid ethyl ester 
• 155191-79-0 1-((E)-5-Bromo-4-methyl-pent-3-enyl)-3-isopropyl-2,5-dimethoxy-benzene 
• 155191-80-3 (E)-5-(3-Isopropyl-2,5-dimethoxy-phenyl)-2-methyl-pent-2-en-1-ol 
• 150267-61-1 3-(3-Isopropyl-2,5-dimethoxy-phenyl)-propionaldehyde 

Relevant academic research and scientific papers

Synthetic studies on diterpenoid quinones with interleukin-1 inhibitory activity. Total synthesis of (±)- and (+)-triptoquinone A

An efficient first total synthesis of (±)- and (+)-triptoquinone A (1), a novel diterpenoid quinone with significant inhibitory activity against interleukin-1 releases, has been completed. Birch reduction of tricyclic enone (±)-7, prepared from known 6-me

Diastereoselective Total Syntheses of (+/-)-Triptoquinone B and C

The first and efficient total syntheses of (+/-)-triptoquinone B 1 and C 2 have been achieved from the allyl ether 3; the key steps are the construction of the four contiguous stereogenic centers present in 2 by the Mn(III) mediated oxidative free radical cyclisation followed by metal hydride reduction.