32774-70-2

Upstream product

• 31929-05-2 3-Acetoxy-2-allyl-2-cyclohexen-1-on 
• 30182-67-3 1,3-Cyclohexanedione 
• 106-95-6 allyl bromide 
• 504-02-9 1,3-cylohexanedione 

Downstream Products

• 69585-88-2 2-Allyl-3-amino-cyclohex-2-enone 
• 50314-05-1 3-chloro-2-(2'-propenyl)cyclohex-2-enone 
• 32774-65-5 2-n-propylcyclohexane-1,3-dione 
• 85696-84-0 3-methoxy-2-(propen-2-yl)cyclohex-2-en-1-one 
• 17605-08-2 2-allyl-3-methyl-2-cyclohexen-1-one 
• 82976-53-2 2-Allyl-3-methylcyclohex-2-enol 
• 82976-49-6 2-Allyl-3-(2-methoxy-ethoxymethoxy)-1-methyl-cyclohexene 
• 150456-45-4 3-Methoxy-6-methyl-2-(2-propenyl)-2-cyclohexenone 
• 1132652-56-2 3-[2,6-dioxo-1-(prop-2-en-1-yl)cyclohexyl]propanal 
• 131375-94-5 4-(3-Oxo-2-propyl-cyclohex-1-enyloxy)-butyric acid ethyl ester 
• 131375-97-8 1-(3-bromopropoxy)2-n-propylcyclohex-1-ene-3-one 
• 105728-95-8 3-(phenylsulfonyl)-2-(2'-propenyl)cyclohex-2-enone 
• 397251-90-0 2-((phenylselanyl)methyl)-3,5,6,7-tetrahydrobenzofuran-4(2H)-one 

Relevant academic research and scientific papers

Enantio- And Diastereoselective Construction of Contiguous Tetrasubstituted Chiral Carbons in Organocatalytic Oxadecalin Synthesis

The organocatalytic enantio- and diastereoselective cycloetherification of 1,3-cyclohexanedione-bearing enones involving the in situ generation of chiral cyanohydrins was developed. This transformation offers the first catalytic asymmetric approach to oxa

A Convenient Synthesis of 2-Alkyl-mono-O-alkylated and 2-Alkyl Resorcinols

The title C,O-dialkylated resorcinols have seldom been prepared.We have developed a practical synthesis of this class of compounds starting with cyclohexane-1,3-dione.The key features of the synthesis are mono-O-alkylation of a 2-alkyl cyclohexane-1,3-dio