137032-93-0

Upstream product

• 137032-61-2 2-Methoxy-1-phenylselanyl-cyclohexanecarbaldehyde 
• 145091-07-2 1-bromo-6-methoxy-cyclohexene 
• 68-12-2 N,N-dimethyl-formamide 
• 61967-21-3 cyclohex-1-ene-1-carbaldehyde dimethyl acetal 
• 1192-88-7 1-cyclohexene-1-carboxaldehyde 
• 50870-61-6 2-bromocyclohex-2-en-1-one 
• 109380-07-6 2-bromocyclohex-2-en-1-ol 

Downstream Products

• 145091-08-3 2-<1-Carbo-tert-butoxyacetyl>-1-methoxy-2-cyclohexene 
• 145091-09-4 2-<1-Carbo-tert-butoxy-2-hydroxyethan-2-yl>-1-methoxy-2-cyclohexene 

Relevant academic research and scientific papers

Stereoselective synthesis of cis-decalins via Diels-Alder and double Michael addition of substituted Nazarov reagents

The base-catalyzed cycloaddition and double Michael cyclization of sustituted Nazarov reagents and 1-phenyl-sulfinyl analogs, with 2-carbomethoxy-2-cyclohexen-1-one 1 yielding cis-decalins is reported.The reaction is highly stereoselective affording cis,c

Facile Access to 2-Alkylidene 3-Oxy Propanals and Propionic Acids from Conjugated Enals

Conjugated enals or their methyl acetals react with benzeneselenyl chloride in the presence of oxygen nucleophile to give Michael-type adducts.The latter are oxidized into 2-alkylidene 3-oxy propanals and propionic acids.