127870-75-1

Upstream product

• 623-27-8 terephthalaldehyde, 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 153680-89-8 1,4-di (3'-isopropylamino-2'-methoxycarbonylprop-1'-enyl) benzene 
• 127923-45-9 2-{Acetoxy-[4-(1-acetoxy-2-methoxycarbonyl-allyl)-phenyl]-methyl}-acrylic acid methyl ester 
• 131469-66-4 C₁₆H₁₄O₈ 

Relevant academic research and scientific papers

Inexpensive ionic liquid mediated green synthetic approach of multi-functionalized regioselective β-lactam fused isoxazolidine heterocyclic hybrids

A novel efficient eco-friendly on “ionic liquid” method has been developed for the synthesis of multi-functionalized isoxazolidines through a nitrone 1,3-dipolar cycloaddition reaction. The low cost and eco-benign room temperature ionic liquid, acetylchol

Synthesis and Structural Features of New Orthocyclophanes, Cyclophanes and Corresponding Macrobicyclic Cryptophanes.

The Baylis-Hillman reaction of dialdehydes with methyl acrylate, followed by acetylation of the resulting diols gave diacetates 3, 14, 16 and 20.Treated with ammonia, these diacetates afforded new cyclophanes and the corresponding macrobicyclic cryptophan

Selective mono and biscondensations of dialdehydes with methylacrylate

DABCO-catalysed mono and biscondensations of dialdehydes with methylacrylate can be easily performed with good to high selectivity under mild conditions.

One-Pot Preparation of 1-Acyl-1-methoxycarbonyloxiranes and 1-Acyl-1-cyanooxiranes from Methyl 3-Hydroxy-2-methylenealkanoates or 3-Aryl-3-hydroxy-2-methylenepropanenitriles

The reaction of sodium hypochlorite with methyl 3-hydroxy-2-methylenealkanoates or 3-aryl-3-hydroxy-2-methylenepropanenitriles, dispersed on silica gel, in acetonitrile leads to oxidation of the alcohol function and epoxidation of the methylene group to g

Synthesis of diaza paracyclophanetetraene and diaza paracyclophanehexaene

The diazabicyclooctane-catalyzed reaction of terephthalaldehyde with methyl acrylate gave the diester 2 or the monoester 4.The diester 2, acetylated and treated with ammonia gave a diaza paracyclophane 6 and the macrobicycle 7.The diester 8, obtaine