6110-30-1Relevant academic research and scientific papers
Efficient two directional syntheses of a homophthalate ester and novel resorcylate oligomers
Patel, Bhavesh H.,Heath, Scott F.A.,Mason, Andrew M.,Barrett, Anthony G.M.
supporting information; experimental part, p. 2258 - 2261 (2011/05/05)
Thermolysis of 6,6′-(2-oxopropane-1,3-diyl)bis(2,2-dimethyl-4H-1,3- dioxin-4-one) in the presence of methanol gave a triketo-ester which subsequently aromatized to provide a synthetically useful homophthalate ester. Enolate C-acylation in the presence of diethylzinc was used to synthesize other double diketo-dioxinones, which on cyclization, aromatization and dioxinone ring opening gave novel double resorcylate derivatives.
Synthesis of 4-hydroxy- and 2,4-dihydroxy-homophthalates by [4+2] cycloaddition of 1,3-bis(silyloxy)-1,3-butadienes with dimethyl allene-1,3-dicarboxylate
Hussain, Ibrar,Yawer, Mirza A.,Appel, Bettina,Sher, Muhammad,Mahal, Ahmed,Villinger, Alexander,Fischer, Christine,Langer, Peter
, p. 8003 - 8009 (2008/12/20)
The reaction of 1,3-bis(trimethylsiloxy)-1,3-butadienes with dimethyl allene-1,3-dicarboxylate provides a convenient and regioselective approach to a variety of functionalized 4-hydroxy- and 2,4-dihydroxy-homophthalates.
A New Approach towards Synthesis of Linear Natural Phenolic Products
Singh, Serjinder,Singh, Iqbal
, p. 586 - 588 (2007/10/02)
A repetitive strategy for the synthesis of linear natural phenolic products involving reaction of two lithium enolate molecules of t-butyl acetate with esters of dicarboxylic acids is reported.
