Photochemical diastereoselective synthesis and spectral characterization of (E)-3-(2-benzoylstyryl)-4H-chromen-4-ones
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Zhigang Xu | Zhong-Zhu Chen | D. Tang | Xiangmei Qu | YuanQi Yu | Hong-Bo Tan | Ze-Hui Qi | Xu Zhang | Bochu Wang | Hong-bo Tan
[1] Rongjie Yang,et al. Analysis on the Caged Structure of Polyhedral Oligomeric Dodecaphenyl Silsesquioxane and Its Condensation Mechanism , 2023, Journal of Molecular Structure.
[2] S. Amano,et al. A Dual Anti-Inflammatory and Anti-Proliferative 3-Styrylchromone Derivative Synergistically Enhances the Anti-Cancer Effects of DNA-Damaging Agents on Colon Cancer Cells by Targeting HMGB1-RAGE-ERK1/2 Signaling , 2022, International journal of molecular sciences.
[3] Zhengjie He,et al. UV Light-Driven Asymmetric Vinylogous Aldol Reaction of Isatins with 2-Alkylbenzophenones and Enantioselective Synthesis of 3-Hydroxyoxindoles , 2022, Organic Chemistry Frontiers.
[4] Xiaonian Li,et al. Structure elucidation, biogenesis, and bioactivities of acylphloroglucinol-derived meroterpenoid enantiomers from Dryopteris crassirhizoma. , 2021, Bioorganic chemistry.
[5] Hongbo Tan,et al. Diastereoselective synthesis and spectral characterization of trans-4,4a-dihydro-3H-benzo[4,5]oxazolo[3,2-a]pyridines , 2021, Journal of Molecular Structure.
[6] F. Uchiumi,et al. A 3-styrylchromone converted from trimebutine 3D pharmacophore possesses dual suppressive effects on RAGE and TLR4 signaling pathways. , 2021, Biochemical and biophysical research communications.
[7] Y. Uesawa,et al. Synthesis and biological evaluation of 3-styrylchromone derivatives as selective monoamine oxidase B inhibitors. , 2021, Bioorganic & medicinal chemistry.
[8] Zhigang Xu,et al. A four-component domino reaction for the synthesis of novel bridgehead nitrogen-containing pyrido[1,2-d][1,4]diazepines , 2021, New Journal of Chemistry.
[9] Hongbo Tan,et al. Synthesis, NMR analysis and X-ray crystal structure of 3,9-bis(4-(trifluoromethyl)phenyl)-3,9-diazatetraasterane , 2020 .
[10] Hongbo Tan,et al. Facile Synthesis of Novel Hexahydroimidazo[1,2-a]pyridine Derivatives by One-pot, Multi-component Reaction under Ambient Conditions. , 2020, ACS combinatorial science.
[11] F. Zhan,et al. Catalyst-Free One-Pot Synthesis of Densely Substituted Pyrazole-Pyrazines as Anti-Colorectal Cancer Agents , 2020, Scientific Reports.
[12] Hongbo Tan,et al. One-pot, multi-component synthesis of ethyl (E)-1-(3-ethoxy-3-oxoprop-1-en-1-yl)-2-aryl-2,5-dihydro-1H-benzo[b][1,4]diazepine-3-carboxylate derivatives , 2020 .
[13] R. Bhatia,et al. Novel p-Functionalized Chromen-4-on-3-yl Chalcones Bearing Astonishing Boronic Acid Moiety as MDM2 Inhibitor: Synthesis, Cytotoxic Evaluation and Simulation Studies. , 2020, Medicinal chemistry (Shariqah (United Arab Emirates)).
[14] Hongbo Tan,et al. Synthesis, NMR analysis and X-ray crystal structure of novel 1,5-dibenzyl-1,2,5,6-tetrahydro-1,5-diazocines , 2019, Journal of Molecular Structure.
[15] Joyce C. Leung,et al. A versatile catalyst system for enantioselective synthesis of 2-substituted 1,4-benzodioxanes† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc05612a , 2019, Chemical science.
[16] P. Melchiorre,et al. Organocatalytic Strategies to Stereoselectively Trap Photochemically Generated Hydroxy‐o‐quinodimethanes , 2018 .
[17] Yong Liang,et al. Synthesis of Benzoaryl-5-yl(2-hydroxyphenyl)methanones via Photoinduced Rearrangement of (E)-3-Arylvinyl-4H-chromen-4-ones. , 2017, Organic letters.
[18] L. Dell’Amico,et al. Forging Fluorine‐Containing Quaternary Stereocenters by a Light‐Driven Organocatalytic Aldol Desymmetrization Process , 2017, Angewandte Chemie.
[19] Hongbo Tan,et al. Synthesis, NMR analysis and X-ray crystal structure of 3-(2-naphthoyl)-6,12-diphenyl-3,9-diazatetraasterane , 2017 .
[20] E. Uriarte,et al. Discovery of New Chemical Entities for Old Targets: Insights on the Lead Optimization of Chromone-Based Monoamine Oxidase B (MAO-B) Inhibitors. , 2016, Journal of medicinal chemistry.
[21] Huiliang Li,et al. Four new isomeric sesquiterpene lactone dimers from Carpesium faberi , 2015 .
[22] M. Banerjee,et al. A Mild and Efficient Route to 3-Vinylchromones in Aqueous Micellar Media , 2015 .
[23] G. Sheldrick. Crystal structure refinement with SHELXL , 2015, Acta crystallographica. Section C, Structural chemistry.
[24] Rangappa S. Keri,et al. Chromones as a privileged scaffold in drug discovery: a review. , 2014, European journal of medicinal chemistry.
[25] J. Cavaleiro,et al. Efficient synthesis of chromones with alkenyl functionalities by the heck reaction , 2010 .
[26] Ting Zhou,et al. Efficient microwave-assisted one-pot preparation of angular 2,2-dimethyl-2H-chromone containing compounds. , 2010, Tetrahedron letters.
[27] Y. Kimura,et al. Enhancing effects of a chromone glycoside, eucryphin, isolated from Astilbe rhizomes on burn wound repair and its mechanism. , 2010, Phytomedicine : international journal of phytotherapy and phytopharmacology.
[28] Y. Mimaki,et al. Chromones from the tubers of Eranthis cilicica and their antioxidant activity. , 2009, Phytochemistry.
[29] Julia K. Hasty,et al. Developing environmentally benign and effective organic wood preservatives by understanding the biocidal and non-biocidal properties of extractives in naturally durable heartwood , 2008 .
[30] J. Jekő,,et al. Microwave-induced synthesis and regio- and stereoselective epoxidation of 3-styrylchromones , 2008 .
[31] Louise N. Dawe,et al. Electron-deficient dienes. 5. An inverse-electron-demand Diels-Alder approach to 2-substituted 4-methoxyxanthones and 3,4-dimethoxyxanthones. , 2008, Organic letters.
[32] A. Gamal-Eldeen,et al. Anti-Cancer and Immunostimulatory Activity of Chromones and Other Constituents from Cassia petersiana , 2007, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[33] Ahmed Awad E. Ahmed,et al. Antitumor and Immunostimulatory Activity of Two Chromones and Other Constituents from Cassia Petersiana , 2006 .