74629-97-3

Upstream product

• 74629-95-1 (1R,2S,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 74629-94-0 (1S,2R,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 34087-39-3 2-(2-oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetonitrile 
• 3886-70-2 (R)-1-(1-Naphthyl)ethylamine 
• 74629-86-0 (+/-)-trans-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)acetic Acid Lactone 

Downstream Products

• 74629-93-9 (1R,2R,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide 
• 74708-32-0 (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide 
• 74629-94-0 (1S,2R,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 74629-95-1 (1R,2S,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 3886-70-2 (R)-1-(1-Naphthyl)ethylamine 
• 74708-21-7 (1R,2R)-(+)-trans-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)acetic Acid Lactone 

Relevant academic research and scientific papers

Enantiomerically Pure Lactones. 2. Approaches to Cis or Trans Multicyclic Lactones

Enantiomerically pure bicyclic lactones 1-3 and tricyclic lactones 4 and 5 have been prepared by either of two procedures, each hinging upon the liquid chromatographic seperation of rationally selected diastereomeric derivatives.After seperation, the diastereomers are converted by a simple high-yield reaction sequence to the enantiomeric multiring lactones, none of which has been previously reported in optically active form. The relative strengths and weaknesses of each approach are discussed.Lactones 4 and 5 were α-methylated, these derivatives being suitable for the determination of enantiomeric purity and absolute configuration using the chiral solvating agent (S)-(+)-2,2,2-trifluoro-1-(9-anthryl)ethanol.