54857-48-6

Usage

Synthesis Reference(s)

Tetrahedron Letters, 17, p. 341, 1976 DOI: 10.1016/S0040-4039(00)93726-2

InChI:InChI=1/C9H16O3/c1-4-12-9(11)6-5-8(10)7(2)3/h7H,4-6H2,1-3H3

Upstream product

• 1068-55-9 isopropylmagnesium chloride 
• 123-25-1 succinic acid diethyl ester 
• 115-19-5 2-methyl-but-3-yn-2-ol 
• 19429-85-7 N,N-dimethylacetamide diethyl acetal 
• 64-17-5 ethanol 
• 3883-58-7 2,2-dimethylcyclopentane-1,3-dione 
• 563-80-4 3-methyl-butan-2-one 
• 95-92-1 oxalic acid diethyl ester 
• 41654-04-0 5-Methyl-4-oxohexanoic acid 
• 140-88-5 ethyl acrylate 
• 94250-54-1 tert-butyl 4-methyl-3-oxopentanoate 
• 14794-31-1 ethyl 3-(chloroformyl)propionate 
• 75-11-6 diiodomethane 
• 7152-15-0 ethyl 4-methyl-3-oxo-pentanoate 

Downstream Products

• 63328-12-1 (5R)-5-(prop-2-yl)pyrrolidin-2-one 
• 78208-72-7 5-(1-methylethyl)-1H-pyrazole-3-carboxylic acid ethyl ester 
• 124865-31-2 Ethyl 2-(4-fluoro-3-phenoxy-benzylidene)-4-methyl-3-oxopentanoate 
• 207236-60-0 (1R*,5S*)-5-isopropyl-8-oxabicyclo[3.2.1]octan-1-ol 
• 41654-04-0 5-Methyl-4-oxohexanoic acid 

Relevant academic research and scientific papers

PHOTOCHEMISTRY OF 1,3-CYCLOPENTANEDIONES. OXETANE FORMATION INVOLVING BOTH ENERGY TRANSFER AND ELECTRON TRANSFER PROCESSES

Photolysis of 2,2-dimethyl-1,3-cyclopentanedione in acetone resulted in oxetane formation in a two photon process involving energy transfer from triplet excited acetone and electron transfer from singlet excited acetone.

From a Designer Drug to the Discovery of Selective Cannabinoid Type 2 Receptor Agonists with Favorable Pharmacokinetic Profiles for the Treatment of Systemic Sclerosis

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Reactions of Propargyl Alcohols with Amide Acetals

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