Novel aurone-type compounds with an extended π-system: Synthesis and optical properties

[1]  M. Z. Hassan,et al.  Aurone: A biologically attractive scaffold as anticancer agent. , 2019, European journal of medicinal chemistry.

[2]  E. Baydoun,et al.  Aurone derivatives as promising antibacterial agents against resistant Gram-positive pathogens. , 2019, European journal of medicinal chemistry.

[3]  Riham F. George,et al.  Aurones and furoaurones: Biological activities and synthesis , 2018, Bulletin of Faculty of Pharmacy, Cairo University.

[4]  Naseem Ahmed,et al.  A Route to Highly Functionalized Stereospecific trans-Aminated Aurones from 3-Bromoflavones with Aniline and N-Phenylurea via a Domino Aza-Michael Ring Opening and Cyclization Reactions , 2018, Synthesis.

[5]  Yunping Liu,et al.  Antioxidant and spectral properties of chalcones and analogous aurones: Theoretical insights , 2018, International Journal of Quantum Chemistry.

[6]  Manish P. Patel,et al.  Antimicrobial and antioxidant evaluation of new quinolone based aurone analogs , 2017 .

[7]  H. Kim,et al.  A novel cyclization/oxidation strategy for a two-step synthesis of (Z)-aurone , 2017 .

[8]  X. Gu,et al.  A novel fluorescent probe based on β-C-glycoside for quantification of bovine serum albumin , 2017 .

[9]  S. Handy,et al.  Antifungal activity of substituted aurones. , 2017, Bioorganic & medicinal chemistry letters.

[10]  X. Gu,et al.  A novel Hg2+-selective fluorescent chemprobe based on thiooxorhodamine-B and β-C-glycoside. , 2017, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[11]  Yan Li,et al.  Synthesis and evaluation of 4-hydroxyl aurone derivatives as multifunctional agents for the treatment of Alzheimer's disease. , 2016, Bioorganic & medicinal chemistry.

[12]  A. Karaburun,et al.  Synthesis and anti-cancer activity evaluation of new aurone derivatives , 2015, Journal of enzyme inhibition and medicinal chemistry.

[13]  H. Tian,et al.  Simultaneous Detection of Diverse Glycoligand‐Receptor Recognitions Using a Single‐Excitation, Dual‐Emission Graphene Composite , 2015 .

[14]  Ana S. Newton,et al.  Probing the aurone scaffold against Plasmodium falciparum: design, synthesis and antimalarial activity. , 2014, European journal of medicinal chemistry.

[15]  Mamdouh M. Ali,et al.  Celecoxib analogs bearing benzofuran moiety as cyclooxygenase-2 inhibitors: design, synthesis and evaluation as potential anti-inflammatory agents. , 2014, European journal of medicinal chemistry.

[16]  L. Altucci,et al.  Novel benzofuran–chromone and –coumarin derivatives: synthesis and biological activity in K562 human leukemia cells , 2013 .

[17]  Mehul A. Patel,et al.  Synthesis of Some 3‐(4‐Aryl‐benzofuro[3,2‐b]pyridin‐2‐yl)coumarins and Their Antimicrobial Screening , 2012 .

[18]  Kamalika Mukherjee,et al.  Aurones: Small Molecule Visible Range Fluorescent Probes Suitable for Biomacromolecules , 2011, Journal of Fluorescence.

[19]  Xin Lu,et al.  Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines. , 2010, European journal of medicinal chemistry.

[20]  Chao‐Jun Li,et al.  Water-triggered, counter-anion-controlled, and silver-phosphines complex-catalyzed stereoselective cascade alkynylation/cyclization of terminal alkynes with salicylaldehydes. , 2009, The Journal of organic chemistry.

[21]  E. Perrier,et al.  Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes. , 2006, Journal of medicinal chemistry.

[22]  A. Boumendjel.  Aurones: a subclass of flavones with promising biological potential. , 2003, Current medicinal chemistry.

[23]  M. Cushman,et al.  A NOVEL OXIDATIVE CYCLIZATION OF 2'-HYDROXYCHALCONES TO 4,5-DIALKOXYAURONES BY THALLIUM(III) NITRATE , 1995 .

[24]  C. Brennan,et al.  Ring closure to ynone systems: 5- and 6-endo- and -exo-dig modes , 1989 .

[25]  J. Eastman,et al.  QUANTITATIVE SPECTROFLUORIMETRY‐THE FLUORESCENCE QUANTUM YIELD OF QUININE SULFATE , 1967 .

[26]  C. A. Parker,et al.  Correction of fluorescence spectra and measurement of fluorescence quantum efficiency , 1960 .

[27]  K. Venkataraman,et al.  387. Synthetical experiments in the chromone group. Part XIV. The action of sodamide on 1-acyloxy-2-acetonaphthones , 1934 .

[28]  W. Baker.  322. Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones , 1933 .