1281445-02-0

Upstream product

• 86211-08-7 S-methyl nonanethioate 
• 6332-83-8 2-(4-chlorophenyl)-1-phenylethanone 
• 32508-91-1 1-phenyl-2-decanone 
• 1387574-34-6 ethyl 4-(2-oxodecyl)benzoate 
• 1387574-33-5 octyl p-cyanophenylmethyl ketone 

Downstream Products

• 1387574-33-5 octyl p-cyanophenylmethyl ketone 
• 1387574-34-6 ethyl 4-(2-oxodecyl)benzoate 
• 32508-91-1 1-phenyl-2-decanone 
• 86211-08-7 S-methyl nonanethioate 
• 67947-51-7 1-(4-chlorophenyl)-2-(2-thienyl)-2-ethanone 
• 727722-44-3 1-[4-(1,1-dimethylethyl)phenyl]-2-(4-chlorophenyl)ethanone 
• 1216134-96-1 1-cyclohexyl-3-(4-chlorophenyl)-2-propanone 
• 17475-40-0 phenyl nonanoate 
• 101554-06-7 2-(4-chlorobenzyl)benzo[d]oxazole 

Relevant academic research and scientific papers

Rhodium-catalyzed acyl-transfer reaction between benzyl ketones and thioesters: Synthesis of unsymmetric ketones by ketone CO-C bond cleavage and intermolecular rearrangement

In the presence of catalytic amounts of RhH(CO)(PPh3) 3 and 1,2-bis(diphenylphosphino)benzene (dppBz), acyl groups were transferred between benzyl ketones and thioesters/aryl esters. The rhodium complex catalyzed the cleavage of keto