123366-53-0

Upstream product

• 110-89-4 piperidine 
• 106-23-0 3,7-dimethyl-oct-6-enal 

Downstream Products

• 106-23-0 3,7-dimethyl-oct-6-enal 
• 107-75-5 7-hydroxy-3,7-dimethyl-octanal 
• 3613-30-7 7-methoxy-3,7-dimethyloctanal 
• 3613-33-0 7-ethoxy-6,7-dihydrocitronellal 
• 69636-81-3 (1R,6R,7R,11R)-(+)-biflora-4,10(19),15-triene 
• 69636-81-3 (1S,6R,7R,11R)-(-)-biflora-4,10(19),15-triene 
• 69636-81-3 (1R,6S,7S,11R)-(+)-biflora-4,10(19),15-triene 
• 69636-81-3 (1S,6S,7S,11R)-(-)-biflora-4,10(19),15-triene 
• 446018-20-8 (1RS,4RS,1′R)-4-(1′,5′-dimethylhex-4′-enyl)-1-methylcyclohex-2-en-1-ol 
• 141-27-5 3,7-dimethyl-2,6-octadienal 
• 106-26-3 cis-3,7-dimethyl-2,6-octadienal 
• 196193-23-4 4-[(1R)-1,5-dimethylhex-4-enyl]cyclohex-2-en-1-one 
• 82451-83-0 2-[3,7-Dimethyl-oct-6-en-(Z)-ylidene]-6-isopropenyl-3-methyl-cyclohexanol 
• 89-79-2 Isopulegol 

Relevant academic research and scientific papers

Kn?lker's iron complex: An efficient in situ generated catalyst for reductive amination of alkyl aldehydes and amines

An aminated series: A well-defined iron-catalyzed reductive amination reaction of aldehydes and ketones with aliphatic amines using molecular hydrogen is presented. Under mild conditions, good yields for a broad range of alkyl ketones as well as aldehydes were achieved. Copyright