59082-30-3Relevant academic research and scientific papers
Michael addition of malononitrile to indenones: Synthesis and characterization of 2-(1-oxo-2,3-dihydro-1H-inden-2-yl) (aryl)(methyl)malononitrile derivatives
?ahin, Betül,Gürdere, Meliha Burcu,Ceylan, Mustafa
, p. 1090 - 1095 (2017/05/25)
Indanones 3 were prepared from the reaction of indanone (1) with corresponding benzaldehyde derivatives 2, as described in the literature. Then, indenones 3 were subjected to KOtBu-catalyzed Michael addition with malononitrile to give a mixture of diaster
p-TSA-promoted syntheses of 5H-benzo[h]thiazolo[2,3-b]quinazoline and indeno[1,2-d]thiazolo[3,2-a]pyrimidine analogs: Molecular modeling and in vitro antitumor activity against hepatocellular carcinoma
Keshari, Amit K.,Singh, Ashok K.,Raj, Vinit,Rai, Amit,Trivedi, Prakruti,Ghosh, Balaram,Kumar, Umesh,Rawat, Atul,Kumar, Dinesh,Saha, Sudipta
, p. 1623 - 1642 (2017/06/19)
In our efforts to address the rising incidence of hepatocellular carcinoma (HCC), we have made a commitment to the synthesis of novel molecules to combat Hep-G2 cells. A facile and highly efficient one-pot, multicomponent reaction has been successfully de
NEW MATERIAL FOR TRANSPORTING ELECTRON AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME
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Paragraph 0071; 0074; 0075, (2016/10/10)
The present invention relates to a novel electron transport material represented by chemical formula 1 and an organic luminescent device using the same. By using the electron transport material, the organic luminescent device which has enhanced luminescent properties and improved electric power consumption by reinforcing driving voltage and inducing increase of power factor can be manufactured.
NEW ELECTRON TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME
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Paragraph 191; 192; 193, (2014/01/07)
Provided are a new electron transport material and an organic electroluminescent device including the same. The electron transport material according to the present invention may have the excellent luminescence property and reduce the driving voltage to increase the power efficiency, such that the organic electroluminescent device using less consumption power may be manufactured.
One-pot inter- and intramolecular Friedel-Crafts reactions in Baylis-Hillman chemistry: A novel facile synthesis of (E)-2-arylideneindan-1-ones
Basavaiah, Deevi,Reddy, Ravi Mallikarjuna
, p. 3025 - 3027 (2007/10/03)
A simple one-pot stereoselective transformation of tert-butyl 3-aryl-3-hydroxy-2-methylenepropanoates, the Baylis-Hillman adducts obtained from t-butyl acrylate, into (E)-2-arylideneindan-1-ones involving one inter- and one intramolecular Friedel-Crafts r
