1,2-aceanthrylenedione

1,2-aceanthrylenedione Structure
1,2-aceanthrylenedione structure
Common Name 1,2-aceanthrylenedione
CAS Number 6373-11-1 Molecular Weight 232.23400
Density 1.433g/cm3 Boiling Point 462.6ºC at 760 mmHg
Molecular Formula C16H8O2 Melting Point 270-273ºC(lit.)
MSDS Chinese USA Flash Point 199.7ºC

Reactions of Acenaphthenequinone and Aceanthrenequinone with Arenes in Superacid.

Appl. Catal. A Gen. 336(1-2) , 128-132, (2008)

The hydroxyalkylation reactions of aceanthrenequinone (6) and acenapthenequinone (7) with a series of arenes have been studied. In reactions with the Br__nsted superacid CF(3)SO(3)H (triflic acid), the condensation products are formed in good yields (58-99%, ...

Planarity and constraint of the carbonyl groups in 1,2-diones are determinants for selective inhibition of human carboxylesterase 1.

J. Med. Chem. 50 , 5727-34, (2007)

Carboxylesterases (CE) are ubiquitous enzymes responsible for the detoxification of xenobiotics, including numerous clinically used drugs. Therefore, the selective inhibition of these proteins may prove useful in modulating drug half-life and bioavailability....

Deoxygenation of some α-dicarbonyl compounds by tris(diethylamino)phosphine in the presence of fullerene C60.

J. Org. Chem. 76(8) , 2548-57, (2011)

The reactions of such cyclic α-diketones as acenaphthenequinone, aceanthrenequinone, and N-alkylisatins, with hexaethyltriaminophosphine in the presence of the fullerene C(60), lead to the formation of methanofullerene derivatives under mild conditions. This ...

MacDonald [2 + 2]-type condensation with vicinal diketones: synthesis and properties of novel spiro-tricyclic porphodimethenes.

Org. Lett. 3(15) , 2281-4, (2001)

[structure: see text] Acid-catalyzed [2 + 2] condensation reactions of polycyclic aromatic vicinal diketones including aceanthrenequinone, phenathrenequinone, and pyrene-4,5-dione with 5-mesityldipyrromethanes are outlined, and this methodology provides a fle...