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Upstream product

• 495394-10-0 (paramethoxybenzylidene)-2 methoxy-6 tetralone-1 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 72861-80-4 (2E)-6-methoxy-2-[(4-methoxyphenyl)methylidene]-3,4-dihydronaphthalen-1-one 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 72862-06-7 4-ethyl-7-methoxy-3-(4-methoxy-benzyl)-1,2-dihydro-naphthalene 
• 77642-60-5 1,2-trans-2-p-methoxybenzyl-1-acetoxy-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-60-5 1,2-cis-1-acetoxy-2-p-methoxybenzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 858199-09-4 1-ethyl-6-methoxy-2-(4-methoxy-benzyl)-naphthalene 
• 872795-12-5 1-ethyl-6-methoxy-2-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-naphthalene 

Relevant academic research and scientific papers

Asymmetric Transfer Hydrogenation of Arylidene-Substituted Chromanones and Tetralones Catalyzed by Noyori-Ikariya Ru(II) Complexes: One-Pot Reduction of C═C and C═O bonds

3-Arylidenechroman-4-ones and 2-arylidene-1-tetralones are hydrogenated to cis-benzylic alcohols in dr's and er's up to 99:1 via a C═C and C═O one-pot reduction in the presence of 2-5 mol % Noyori-Ikariya-type RuII chiral complexes and HCO2Na as a hydroge

Studies in Antifertility Agents: Part XXVIII-1,2-trans-1-(p-(&β-Pyrrolidinoethoxy)phenyl)-2-substituted-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalenes

Substituted 2-benzyl-6-methoxy-1-tetralones (8-10), obtained by catalytic hydrogenation of 2-arylidene-1-tetralones (5-7), on NaBH4 reduction give a mixture of 1,2-trans-/cis-isomers of 2-benzyl-1-tetralols (11-13).Ac2O-pyridine treatment of 11 furnishes