137758-96-4

Upstream product

• 150267-58-6 2-Allyl-4-methoxy-6-isopropylphenol 
• 150267-57-5 Allyl 4-methoxy-2-isopropylphenyl ether 
• 150267-59-7 1-Allyl-2,5-dimethoxy-3-isopropylbenzene 
• 1629-58-9 4-penten-3-one 
• 155191-03-0 1,4-Dimethoxy-5-methyl-2-isopropyl-7,8-dihydronaphthalene 
• 155191-00-7 4-(2,5-Dimethoxy-3-isopropylphenyl)butyraldehyde 
• 153341-13-0 Allyl 4-bromo-2-isopropylphenyl ether 
• 146356-67-4 (4aS^*,10aR^*)-5,8-Dimethoxy-1,4a-dimethyl-7-isopropyl-2-(trifluoromethanesulfonyloxy)-3,4,4a,9,10,10a-hexahydrophenanthrene 
• 146356-66-3 (4aS^*,10aR^*)-5,8-Dimethoxy-1,4a-dimethyl-7-isopropyl-2-((trimethylsilyl)oxy)-3,4,4a,9,10,10a-hexahydrophenanthrene 
• 162920-92-5 5,8-Dimethoxy-1,4a-dimethyl-7-isopropyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrenone 
• 146356-64-1 5,8-Dimethoxy-6-isopropyl-1-methyl-2-tetralone 
• 146356-63-0 5,8-Dimethoxy-6-isopropyl-2-tetralone 
• 146356-62-9 2-isopropyl-1,4,6-trimethoxynaphthalene 
• 146356-61-8 4-Bromo-2-isopropyl-1,6-dimethoxynaphthalene 

Relevant academic research and scientific papers

TOTAL SYNTHESIS OF (+/-)-TRIPTOQUINONE A

A concise and practical total synthesis of (+/-)-triptoquinone A (1), a novel interleukin-1 inhibitor isolated from Tripterygium wilfordii var. regelii, has been achieved in 11 steps from the known naphthol 2.

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