681292-99-9

Upstream product

• 681292-90-0 (E)-5-(2-Benzyloxymethyl-cyclopropyl)-pent-4-enoic acid ethyl ester 
• 681293-10-7 [2-((E)-5-Azido-pent-1-enyl)-cyclopropylmethoxymethyl]-benzene 
• 681292-91-1 (E)-5-(2-Benzyloxymethyl-cyclopropyl)-pent-4-en-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 201230-82-2 carbon monoxide 
• 681292-93-3 N-[5-(2-benzyloxymethyl-cyclopropyl)-pent-4-enyl]-4-methyl-benzenesulfonamide 

Relevant academic research and scientific papers

2,5-Dialkyl Cyclohexenones by Fe(CO)5-Mediated Carbonylation of Alkenyl Cyclopropanes: Functional Group Compatibility

The preparation of alkenyl cyclopropanes 1 with a variety of common organic functionalities is reported. These substrates were subjected to the Fe(CO)5-mediated carbonylation process under a CO atmosphere, leading to the formation of 2,5-disubstituted cyclohexenones 2, important intermediates for target-directed synthesis.