74796-40-0

Upstream product

• 74796-26-2 2,2-dimethyl-5-(1-methyl-2-hydroxypropyl)-3(2H)-furanone 
• 74796-28-4 2,2-dimethyl-5-(1-methyl-2-hydroxy-2-phenylethyl)-3(2H)-furanone 
• 18458-23-6 2,2-dimethyl-5-ethyl-furan-3(2H)-one 
• 115-22-0 3-Hydroxy-3-methyl-2-butanone 
• 55816-60-9 3-methyl-3-<(trimethylsilyl)oxy>-2-butanone 
• 75767-42-9 5-hydroxy-2-methyl-2-<(trimethylsilyl)oxy>-3-heptanone 
• 75767-43-0 2-methyl-2-<(trimethylsilyl)oxy>-3,5-heptanedione 
• 100-52-7 benzaldehyde 
• 110841-44-6 [1-(5,5-Dimethyl-4-oxo-4,5-dihydro-furan-2-yl)-ethyl]-phosphonic acid diethyl ester 
• 110841-48-0 [5-(1-Hydroxy-1-methyl-ethyl)-isoxazol-3-ylmethyl]-phosphonic acid diethyl ester 
• 110841-49-1 {1-[5-(1-Hydroxy-1-methyl-ethyl)-isoxazol-3-yl]-ethyl}-phosphonic acid diethyl ester 

Relevant academic research and scientific papers

An Entry to 5-(1-Alkenyl)-3(2H)-furanones through Cycloaddition of Phosphorus-Functionalized Nitrile Oxide to Acetylene Alcohols. An Effective Synthesis of Geiparvarin

Cycloaddition of α-(diethoxyphosphoryl)acetonitrile oxide to acetylene alcohols is followed by an alkylation, a reductive cleavage of the N-O bond, and an acid-catalyzed cyclization to form 5-(diethoxyphosphorylmethyl)-3(2H)-furanones in good yields.Subse

Synthesis and Configurational Assignment of Geiparvarin: A Novel Antitumor Agent

This report presents the first total synthesis of geiparvarin as well as assignment of configuration of the previously undefined trisubstituted olefin.A central aspect of this synthetic adventure leading to this novel antitumor agent which possesses the 3