75700-18-4

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 67705-11-7 3-<(E)-1-hexenyl>-2-cyclohexenone 
• 132079-99-3 3-((Z)-Hex-1-en-1-yl)-2-cyclohexenone 
• 75700-19-5 3-(benzylsulfanyl)cyclohex-2-en-1-one 
• 10345-87-6 3-phenylcyclohex-2-enone 
• 118716-39-5 3-(1-butoxyvinyl)-cyclohex-2-enone 
• 156812-61-2 Allyl-[2-(3-methoxy-cyclohex-1-enylsulfanyl)-phenyl]-dimethyl-silane 
• 156812-62-3 Allyl-[2-(3-methoxy-cyclohex-1-enesulfonyl)-phenyl]-dimethyl-silane 
• 52035-03-7 3-(chloromethyl)cyclohex-2-en-1-one 
• 872452-02-3 N-(1-(3-oxocyclohex-1-enyl)vinyl)acetamide 
• 6135-22-4 3-(dimethylamino)cyclohex-2-en-1-one 
• 81036-91-1 3-(α-hydroxybenzyl)-2-cyclohexen-1-one 
• 56671-81-9 3-bromo-2-cyclohexen-1-one 
• 56671-82-0 3-Iodocyclohex-2-enone 

Relevant academic research and scientific papers

Total Synthesis of Benzofuran-Based Aspergillusene B via Halogenative Aromatization of Enones

A novel "non-aromatic pool" synthetic strategy for the synthesis of benzofuran-based natural products via oxidative haloaromatization of enones is reported. This approach is successfully applied in the first total synthesis of the natural product aspergil

PYRIDONE DERIVATIVE HAVING AFFINITY FOR CANNABINOID 2-TYPE RECEPTOR

It was found that the compound having a binding activity to the cannabinoid type 2 receptor represented by the formula (I): wherein R' is a group represented by the formula: -Y1-Y2-Y3Ra wherein Y1 is single bond or the like; Y2 is -C(=O)-NH- or the like; Y3 is optionally substituted aryl or the like; R2 is hydrogen or the like; R3 is alkyl or the like; R4 is alkyl or the like; R5 is optionally substituted alkyl or the like; or R3 and R4 taken together with the adjacent atom form cyclic group or the like.