76000-62-9

Upstream product

• 65844-58-8 2-benzyl-5-methoxy-2,3-dihydro-1H-inden-1-one 
• 100-52-7 benzaldehyde 
• 75258-84-3 (E)-2-benzylidene-5-methoxy-2,3-dihydro-1H-inden-1-one 
• 5111-70-6 5-methoxy-1-indanone 

Downstream Products

• 76000-76-5 1--5-methoxyindane 
• 76000-77-6 1--5-methoxyindane 
• 76000-74-3 Acetic acid 2-(2-benzyl-5-methoxy-indan-1-yl)-phenyl ester 
• 76000-72-1 Acetic acid 4-((1S,2S)-2-benzyl-5-methoxy-indan-1-yl)-phenyl ester 
• 831171-87-0 4-methoxy-2-(2-oxo-3-phenylpropyl)benzaldehyde 
• 831171-85-8 2-benzyl-5-methoxy-1H-indene 
• 76000-68-5 4-((1S,2S)-2-Benzyl-5-methoxy-indan-1-yl)-phenol 
• 76000-70-9 2-(2-Benzyl-5-methoxy-indan-1-yl)-phenol 
• 345292-72-0 2-benzyl-5-methoxy-1-acetoxyindan 

Relevant academic research and scientific papers

Studies on the chemistry of 2-(2-oxo-3-phenylpropyl)-benzaldehydes: Novel total synthesis of 3-phenylnaphthalen-2-ols and 2-hydroxy-3-phenyl-1,4- naphthoquinones

We describe the first studies on the chemistry of 2-(2-oxo-3-phenylpropyl) benzaldehydes, which were converted into 3-benzylisochromen-1-ones via the corresponding 2-(2-oxo-3-phenylpropyl)benzoic acid. The 2-(2-oxo-3-phenylpropyl) benzaldehydes proved to be convenient starting materials for the synthesis of 3-phenyl-2-naphthols. Oxidation of the latter compounds resulted in a novel, efficient synthesis of 3-phenyl-1,2-naphthoquinones, which were efficiently transformed into 2-hydroxy-3-phenyl-1,4-naphthoquinones.

Studies in Antifertility Agents: Part XXVI - Synthesis of 1--2-benzyl-5- and 6-methoxyindanes

2-Benzyl-5- and 6-methoxyindan-1-ones (5,6), prepared by catalytic hydrogenation of 2-benzylideneindan-1-ones (3,4) on KBH4 reduction give 2-benzylindan-1-ols (7,8).Friedel-Crafts acetylation of 7 and 8 with phenol results in a mixture of 1-(o- and p-hydr