87141-69-3

Upstream product

• 90359-85-6 1-Cyclopropyl-3-(m-methoxyphenyl)propyl alcohol 
• 344334-33-4 1-Cyclopropyl-3-(3-methoxy-phenyl)-propan-1-one 
• 87141-68-2 ethyl 3-cyclopropyl-2-(3-methoxybenzyl)-3-oxopropanoate 
• 874-98-6 1-bromomethyl-3-methoxybenzene 
• 24922-02-9 Ethyl 3-cyclopropyl-3-oxopropionate 
• 765-43-5 Cyclopropyl methyl ketone 
• 90359-83-4 (Z)-1-Cyclopropyl-3-(3-methoxy-phenyl)-propenone 
• 90359-84-5 (Z)-1-Cyclopropyl-3-(3-methoxy-phenyl)-prop-2-en-1-ol 
• 591-31-1 3-methoxy-benzaldehyde 

Downstream Products

• 69253-49-2 1-((E)-6-Bromo-hex-3-enyl)-3-methoxy-benzene 
• 75682-90-5 1-[(E)-6-(3-Methoxy-phenyl)-hex-3-enyl]-6-methyl-7-oxa-bicyclo[4.1.0]heptan-2-one 
• 75682-87-0 2-[(E)-6-(3-Methoxy-phenyl)-hex-3-enyl]-3-methyl-cyclohex-2-enone 

Relevant academic research and scientific papers

Synthesis of Steroids: Part IX - A New Approach Towards Synthesis of Estrone, 6-Thiaestrone and Their D-Homo Analogues

A new approach for the synthesis of estrone, 6-thiaestrone and their D-homo-analogues is described.This involves preparation of homoallyl halides (XIIIa, b) and C-alkylation of 2-methylcyclohexane-1,3-dione (Va) followed by cyclodehydration to the steroid

3-Methylcyclohex-2-enone Derivatives as Initiators of Cyclisation. Part 4. Some Bicyclisations

Hydrochrysene and hydrophenanthrene derivatives (8)-(14) have been prepared by cyclisation of 2-substituted 3-methylcyclohexen-2-ones and the derived 2,3-epoxides.Cyclisation of the epoxides does not give preparatively useful yields of bicyclised compound