1007392-17-7

Upstream product

• 2033-24-1 cycl-isopropylidene malonate 
• 1571-08-0 methyl 4-formylbenzoate 

Downstream Products

• 1007392-43-9 methyl 4-((2E)-1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(ethoxycarbonyloxy)but-2-enyl)benzoate 
• 1007392-30-4 methyl 4-((2E)-4-acetoxy-1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)but-2-enyl)benzoate 
• 1189171-14-9 methyl 4-(1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-3-(trimethylsilyl)prop-2-ynyl)benzoate 
• 1204474-06-5 (S)-methyl 4-(1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)but-2-ynyl)benzoate 

Relevant academic research and scientific papers

Enantioselective rhodium-catalyzed conjugate alkynylation of 5-benzylidene Meldrum's acids with TMS-acetylene

(Chemical Equation Presented) The enantioselective alkynylation of benzylidene Meldrum's acids has been successfully achieved through rhodium-catalyzed addition of TMS-acetylene in the presence of bisphosphine ligand 3,5-Xylyl-MeOBIPHEP. The resulting Mel

Sequential Rh(l)/Pd-catalyzed 1,4-addition/Lntramolecular allylation: Stereocontrolled construction of γ-butyrolactones and cyclopropanes

The rhodium-catalyzed conjugate addition of functionalized vinyltin reagents to alkylidene Meldrum's acids, followed by Pd-catalyzed intramolecular allylation, is a direct entry into vinyl-substituted y-lactones via Oalkylation and vinylcyclopropanes via