73739-84-1

Upstream product

• 111950-25-5 1-hydroxy-4,6-dimethyl-7-oxo-4-phenyl-2,3-dioxabicyclo<4.3.0>nonane 
• 74766-13-5 2-(3-bromo-2-oxopropyl)-2-methylcyclopentane-1,3-dione 
• 603-35-0 triphenylphosphine 

Downstream Products

• 116458-78-7 6a-Hydroxy-2,3a-dimethyl-3a,5,6,6a-tetrahydro-3H-cyclopenta[b]pyrrol-4-one 
• 151359-31-8 3-Acetyl-4-hydroxy-2-methyl-cyclohex-3-enone 

Relevant academic research and scientific papers

Synthesis and derivatization of bis-nor Wieland-Miescher ketone

An efficient synthesis of bis-nor Wieland-Miescher ketone and its derivatives starting from commercially available 2-allyl-2-methylcyclopenta-1,3- dione is described. Georg Thieme Verlag Stuttgart.

Formal Cycloaddition of Molecular Oxygen, 1,3-Diketone, and Olefin. Synthesis and Reactions of Cyclic Peroxides

Formal cycloaddition of molecular oxygen, 1,3-diketones, and olefins took place by electrochemical oxidation.A catalytic amount of electricity was sufficient for the reaction, and an electroinitiated radical chain mechanism was proposed.The reaction was also initiated by a radical initiator.The resulting cyclic peroxides reacted with acids and some reducing agents such as ferrous sulfate, thiurea, and copper(I) chloride to give oxygen-oxygen bond cleavage products.