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Upstream product

• 96306-50-2 3,3′-(phenylmethylene)bis(2-hydroxynaphthalene-1,4-dione) 
• 83-72-7 2-hydroxynaphtho-1,4-quinone 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

Graphene Oxide Incorporated Strontium Nanoparticles as a Highly Efficient and Green Acid Catalyst for One-Pot Synthesis of Tetramethyl-9-aryl-hexahydroxanthenes and 13-Aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones Under Solvent-Free Conditions

An efficient, inexpensive and recyclable graphene oxide/strontium nanocatalyst was synthesized and applied in a pseudo three-component, one-pot cyclocondensation of aromatic aldehydes and dimedone/lowson to afford the corresponding 3,3,6,6-tetramethyl-9-a

Immobilized copper-layered nickel ferrite on acid-activated montmorillonite, [(NiFe2O4?Cu)(H+-Mont)], as a superior magnetic nanocatalyst for the green synthesis of xanthene derivatives

In this study, the immobilization of copper-layered nickel ferrite on the surface and in the cavities of acid-activated montmorillonite (H+-Mont) was investigated. In this context, magnetic nanoparticles (MNPs) of NiFe2O4

Catalytic application of a nano-molten salt catalyst in the synthesis of biological naphthoquinone-based compounds

In this investigation, a new application of 1H-imidazol-3-ium tricyanomethanide catalyst was explored. The catalyst presented a robust catalytic applicability for the preparation of naphthoquinone-based compounds under mild and green reaction conditions.

Trityl bromide versus nano-magnetic catalyst in the synthesis of henna-based xanthenes and bis-coumarins

Abstract: In this work, trityl bromide (TrBr) as a new, efficient, mild and neutral catalyst was used for the synthesis of henna-based xanthenes (aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones) and bis-coumarins by in situ generation of trityl carb

Choline chloride and itaconic acid-based deep eutectic solvent as an efficient and reusable medium for the preparation of 13-aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones

Choline chloride and itaconic acid-based deep eutectic solvent has been identified as an effective catalyst and reaction medium for synthesis of 13-aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones by condensation of 2-hydroxynaphthalene-1,4-dione wit

N-Sulfonic acid poly(4-vinylpyridinium) hydrogen sulfate as an efficient and reusable solid acid catalyst for one-pot synthesis of xanthene derivatives in dry media under ultrasound irradiation

N-Sulfonic acid poly(4-vinylpyridinium) hydrogen sulfate catalyzed efficiently the synthesis of xanthene derivatives under ultrasonic irradiation at room temperature, which has prompted various concerns involving cost and environmental persistence. This methodology shows the effect of presence of anion hydrogen sulfate as an important and effective factor on the promotion of the one-pot multi-components and condensation reactions. The catalyst can be recovered by simple filtration and used for several times without a significant loss of catalytic activity.

New basic ionic liquid from ethan-1,2-diyl bis (hydrogen sulfate) and DBU (1,8-diazobicyclo[5.4.0]undec-7-ene) as an efficient catalyst for one-pot synthesis of xanthene derivatives

For the first time a new basic ionic liquid from ethan-1,2-diyl-bis (hydrogen sulfate) and 1,8-diazobicyclo[5.4.0]undec-7-ene was suggested. The catalytic activity of the new ionic liquid was tested for synthesis of xanthene derivatives by condensation of aldehydes with i) dimedone ii) β-naphthol iii) 2-hydroxynaphthalene-1,4-dione iv) dimedone and β-naphthol v) 2-hydroxynaphthalene-1,4-dione and dimedone vi) β-naphthol and 2-hydroxynaphthalene-1,4-dione. This approach is a clean, environmentally friendly and convenient work up protocol. The new ionic liquid is an effective and inexpensive catalyst that could easily be recycled and reused five times without significant loss of catalytic activity.

ZrOCl2·8H2O as an efficient catalyst for the synthesis of dibenzo [b,i]xanthene-tetraones and fluorescent hydroxyl naphthalene-1,4-diones

Abstract An efficient and environmentally benign protocol for the synthesis of dibenzo [b,i]xanthene-tetraones and fluorescent hydroxyl naphthalene-1,4-diones in the presence of a catalytic amount of ZrOCl2·8H2O as an inexpensive and eco-friendly catalyst with high catalytic activity under solvent-free conditions is reported. Graphical abstract: [Figure not available: see fulltext.]

Zn(L -proline)2 as a powerful and reusable organometallic catalyst for the very fast synthesis of 2-amino-4H-benzo[g]chromene derivatives under solvent-free conditions

An efficient route for the synthesis of 2-amino-4H-benzo[g]chromenes via a three-component coupling reaction of aldehydes, malononitrile and 2-hydroxy-1,4-naphthaquinone in the presence of Zn(L-proline)2 is reported. High yields, short reaction

Br?nsted acidic ionic liquids catalyzed the preparation of 13-aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones and 3,4-dihydro-1H-benzo[b]xanthene-1,6,11(2H,12H)-triones

An environmentally green method for the synthesis of 13-aryl-5H-dibenzo[b, i]xanthene-5,7,12,14(13H)-tetraone and 3,4-dihydro-1H-benzo[b]xanthene-1,6, 11(2H,12H)-trione derivatives using Br?nsted acidic ionic liquids, 3-methyl-1-sulfonic acid imidazolium chloride, 1-H-3-methyl-imidazolium hydrogensulfate, triethylamine-bonded sulfonic acid, and triethylammonium hydrogensulfate as reusable catalysts under thermal solvent-free conditions is described.