160962-08-3

Upstream product

• 252864-88-3 (1R,2S)-trans-2-isopropyl-1,2-dihydronaphthalene-1-acetaldehyde 
• 252864-82-7 (1R,2S)-trans-2-isopropyl-1-(2-methoxyvinyl)-1,2-dihydronaphthalene 
• 160962-05-0 (1R,2S)-trans-2-isopropyl-1,2-dihydronaphthalene-1-carboxaldehyde 
• 252865-08-0 (1R,2S)-trans-1-[2-(benzoylamino)ethyl]-2-isopropyl-1,2-dihydronaphthalene 
• 252865-05-7 (1R,2S)-trans-1-(cyanomethyl)-2-isopropyl-1,2-dihydronaphthalene 
• 99797-49-6 (+)-trans-1-(hydroxymethyl)-2-isopropyl-1,2-dihydronaphthalene 
• 252864-72-5 (4R)-2-(1-Naphthyl)-4-phenyl-1,3-oxazolidine 
• 252864-99-6 Benzyl-[2-((1R,2S)-2-isopropyl-1,2-dihydro-naphthalen-1-yl)-ethyl]-amine 

Relevant academic research and scientific papers

Asymmetric synthesis of 9-alkyl-2-benzyl-6,7-benzomorphans: Characterization as novel σ receptor ligands

A convenient enantioselective synthesis of (1R,5R,9R)- and (1S,5S,9S)-9- alkyl-2-benzyl-6,7-benzomorphans (2a-c) which starts with naphthaldehyde is described. These compounds were designed to gain additional information on the structure-σ binding relatio

A novel asymmetric synthesis of 3-Benzyl-1,2,3,4,5,6-hexahydro-11-alkyl-2,6-methano-3- benzazocines

9-Alkyl 6,7-benzomorphans (1,2,3,4,5,6-hexahydro-11-alkyl-2,6-methano-3-benzazocines) are important selective ligands of sigma receptor sites; their asymmetric synthesis starting with (1 R,2R)- or (1S,2S)-1-hydroxymethyl-2-alkyl-1,2-dihydronaphthalene is