99797-36-1

Upstream product

• 51594-34-4 (1S,2S)-2-amino-3-methoxy-1-phenyl-1-propanol 
• 97050-27-6 5-methoxy-1-naphthamide 
• 51934-37-3 5-methoxy-1-naphthoic acid 
• 110173-98-3 5-methoxy-[1]naphthoyl chloride 

Downstream Products

• 110174-05-5 (+)-trans-1-<(benzyloxy)methyl>-2-vinyl-5-methoxy-1,2-dihydronaphthalene 
• 110174-12-4 1-<(benzyloxy)methyl>-2-ethyl-2-hydroxy-5-methoxy-1,2,3,4-tetrahydronaphthalene 
• 110174-08-8 (1R,2S)-1-Benzyloxymethyl-2-(1-hydroxy-ethyl)-5-methoxy-1,2,3,4-tetrahydro-naphthalen-2-ol 
• 110174-07-7 1-<(benzyloxy)methyl>-2-acetyl-2-hydroxy-5-methoxy-1,2,3,4-tetrahydronaphthalene 
• 110174-06-6 1-<(benzyloxy)methyl>-2-acetyl-2-hydroxy-5-methoxy-1,2-dihydronaphthalene 
• 110174-18-0 (1S,2S,4R)-2-Ethyl-2-hydroxy-5-methoxy-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid methyl ester 
• 110174-18-0 (1R,2R,4S)-2-Ethyl-2-hydroxy-5-methoxy-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid methyl ester 
• 114838-81-2 1α-methyl-1β-oxazolinyl-2β-(4-pentenyl)-3,4-dehydro-5-methoxy-tetralin 

Relevant academic research and scientific papers

Asymmetric Additions to Chiral Naphthalenes. 4. An Asymmetric Synthesis of the AB-Ring of Aklavinone

The chiral 1-naphthyloxazoline (+)-6, prepared from known 1-iodo-5-methoxynaphthalene, was treated with vinyllithium to afford the dihydronaphthalene 8, after quenching and reductive removal of the chiral auxiliary.Introduction of the tertiary hydroxyl gr