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Upstream product

• 83586-04-3 7t-Methyl-(3arH,7atH)-3a,4,7,7a-tetrahydro-indanon-⁽¹⁾ 
• 2004-70-8 1-methylbuta-1,3-diene 
• 605686-10-0 7t-Methyl-(3arH,7acH)-3a,4,7,7a-tetrahydro-indanon-⁽¹⁾ 
• 22627-64-1 2-Methyl-3-(penten-4-yl)-cyclopentanon 
• 34164-50-6 4-penten-1-ylmagnesium bromide 
• 22627-62-9 3-(4-pentenyl)-2-methyl-2-cyclopentenone 
• 930-30-3 cyclopent-2-enone 
• 22627-65-2 2-Methyl-3-(4-brom-pentyl)-cyclopentanon 

Relevant academic research and scientific papers

Silicon-Directed Nazarov Reactions III. Stereochemical and Mechanistic Considerations

The influence of remote substituents on the stereochemical outcome of electrocyclization in the silicon-directed Nazarov reaction has been examined.While the degree of stereocontrol was modest (ca. 3:1) the substituent in the major isomer (4,5 or 7-substi

Diels-Alder Reactions of Cycloalkenones. 1. Preparation and Structure of the Adducts

Uncatalyzed and aluminum chloride induced Diels-Alder reactions of 2-cyclopentenones, 2-cyclohexenones, and 2-cycloheptenones with 1,3-butadiene, isoprene, and (E)-piperylene are described.Structure analysis of the adducts and their hydrogenation products by standard means and 13C NMR spectroscopy is presented.