1246650-33-8

Upstream product

• 533-31-3 Sesamol 
• 99-61-6 3-nitro-benzaldehyde 
• 126-81-8 dimedone 

Relevant academic research and scientific papers

HClO4-SiO2-catalyzed synthesis of 12-aryl-12H-benzo[i][1,3]dioxolo[4,5-b]xanthene-6,11-diones and 10-aryl-6,7,8,10-tetrahydro-7,7-dimethyl-9h-[1,3]dioxolo[4,5-b]xanthen-9-ones

Three-component one-pot synthesis of some novel 12-aryl-12H-benzo[i][1,3] dioxolo[4,5-b]xanthene-6,11-diones involving treatment of 3,4- methylenedioxyphenol, aldehydes, and 2-hydroxy-1,4-naphthoquinone in presence of HClO4-SiO2 was

Activated carbon/moo3: Efficient catalyst for green synthesis of chro-meno[d]pyrimidinediones and xanthenones

Background: Nanoscale metal oxide catalysts have been extensively employed in organic reactions because they have been found to influence the chemical and physical properties of bulk material. The chromene (benzopyran) nucleus constitutes the core structu

A green synthesis of Xanthenone derivatives in aqueous media using TiO2-CNTs Nanocomposite as an Eco-Friendly and Re-Usable Catalyst

Aim and Objective: The xanthene (dibenzopyran) framework constitutes the core structure of many biologically active compounds, that they have been of interest because of their pharmacological activities like antiviral, antibacterial, anti-inflammatory, an

Cyclodextrin nanosponges: a potential catalyst and catalyst support for synthesis of xanthenes

The nanoporous framework of a cyclodextrin nanosponge was used as catalyst for accelerating the one-pot, three-component reaction of dimedone, aldehyde, and phenols for synthesis of xanthene derivatives. Moreover, the nanocavities of cyclodextrin nanospon

Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid

Dimedone reacted with aromatic aldehydes and 3,4-methylenedioxyphenol or β-naphthol in the presence of a catalytic amount of Preyssler type heteropolyacid, H14[NaP5W30O110], as a green and reusable catalyst unde