16626-54-3

Upstream product

• 42330-88-1 1-chloro-3-(2-tetrahydropyranyloxy)propane 
• 100-45-8 3-cyclohexene-1-carbonitrile 
• 201230-82-2 carbon monoxide 
• 100-40-3 4-ethenylcyclohexene 
• 22482-62-8 3-(cyclohex-3-en-1-yl)propanoic acid 
• 766-03-0 3-vinylcyclohexene 
• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 72581-32-9 cyclohex-3-enylmethanol 
• 78640-15-0 3-(3-Cyclohexen-1-yl)propansaeure-methylester 
• 75-21-8 oxirane 
• 2555-08-0 4-(chloromethyl)cyclohex-1-ene 

Downstream Products

• 1124-63-6 3-cyclohexylpropan-1-ol 
• 22482-62-8 3-(cyclohex-3-en-1-yl)propanoic acid 
• 22858-74-8 3-(cyclohex-3-en-1-yl)propanal 
• 280-65-9 bicyclo[3.3.1]nonane 
• 6671-66-5 bicyclo[3.3.1]non-2-ene 
• 2568-17-4 bicyclo[3.3.1]nonan-2-one 
• 22482-52-6 3-(3-Cyclohexen-1-yl)-propionsaeurechlorid 

Relevant academic research and scientific papers

Tandem rhodium-catalyzed hydroformylation-hydrogenation of alkenes by employing a cooperative ligand system

Dual action: A multifunctional rhodium catalyst system enables the simultaneous catalysis of two distinct transformations, hydroformylation of an alkene and reduction of an aldehyde, in a highly selective manner. This one-pot/two-step process is controlled by the cooperative action of two different supramolecular ligand systems and transforms terminal alkenes into C1-chain-elongated linear alcohols. Copyright

Reductive Carbonylation of Alkenes using Zwitterionic Rhodium Complexes as Catalysts

Alkenes react with carbon monoxide, sodium borohydride, propan-2-ol and a catalytic amount of Rh(cod)(η6-PhBPh3) (cod = cyclooctadiene) to give alcohols in fine yields; high regioselectivity for the branched or linear alcohol is usually observed, depending on the organic substrate.