124568-69-0

Upstream product

• 120-72-9 indole 
• 135630-37-4 5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 102720-24-1 Indole-3-magnesium iodide 
• 120094-31-7 6-Oxo-7,7,9-trimethyl-5,6,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 120094-32-8 6α-Hydroxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 124549-82-2 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid 
• 120094-31-7 6-Oxo-7,7-9-trimethyl-5,6,6aα,7,8,10αβ-hexahydroindeno-<2,1-b>indole 
• 124549-81-1 2β-Benzoxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic benzoic anhydride 
• 78-59-1 3,5,5-Trimethylcyclohex-2-en-1-one 
• 124549-80-0 2β-Hydroxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylate 

Relevant academic research and scientific papers

A general approach to the total synthesis of yuehchukene and its analogues. A novel anti-implantation agent

A versatile synthetic strategy has been developed for the synthesis of the interesting dimeric indole natural product yuehchukene (17) and its epimer, 6a-epi-yuehchukene (22). Due to the anti-implantation activity associated with 17, it is important to develop a synthetic route not only to 17, but to a family of yuehchukene analogues with better chemical stability and/or elevated biological activity. The strategy described here and which utilizes the readily available and inexpensive isophorone (1) satisfies these requirements.