Synthesis of 4-styrylcoumarins via FeCl3-promoted cascade reactions of propargylamines with β-keto esters.
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Hui Wang | Xinwei He | Y. Shang | Mengqing Xie | Youpeng Zuo | Xiaoting Cai | Li-Qin Yan | Xinwei He | Liqin Yan
[1] Da-qi Wang,et al. Lewis Acid Catalyzed Tandem 1,4-Conjugate Addition/Cyclization of in Situ Generated Alkynyl o-Quinone Methides and Electron-Rich Phenols: Synthesis of Dioxabicyclo[3.3.1]nonane Skeletons. , 2018, Organic letters.
[2] Vsevolod A. Peshkov,et al. Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles. , 2018, Chemical Society reviews.
[3] Yuanchao Lv,et al. Solid-state fluorescent materials based on coumarin derivatives: polymorphism, stimuli-responsive emission, self-assembly and optical waveguides , 2018 .
[4] Z. Mao,et al. A coumarin Schiff's base two-photon fluorescent probe for hypochlorite in living cells and zebrafish , 2018, RSC advances.
[5] Z. Jing,et al. Base-catalysed [3 + 2] cycloaddition of propargylamines and aldehydes to substituted furans , 2018 .
[6] Ji-Yuan Du,et al. Metal-Free One-Pot Synthesis of 3-Phosphinoylbenzofurans via Phospha-Michael Addition/Cyclization of H-Phosphine Oxides and in Situ Generated ortho-Quinone Methides. , 2018, Organic letters.
[7] D. Castagnolo,et al. Synthesis and Reactivity of Propargylamines in Organic Chemistry. , 2017, Chemical reviews.
[8] Zhi Xu,et al. Recent developments of coumarin-containing derivatives and their anti-tubercular activity. , 2017, European journal of medicinal chemistry.
[9] Amol S. Kotmale,et al. Coumarin-Appended Stable Fluorescent Self-Complementary Quadruple-Hydrogen-Bonded Molecular Duplexes. , 2017, The Journal of organic chemistry.
[10] S. N. Bukhari,et al. Coumarins scaffolds as COX inhibitors. , 2017, Bioorganic chemistry.
[11] A. Bekhradnia,et al. New protocols to access imidazoles and their ring fused analogues: synthesis from N-propargylamines , 2017 .
[12] M. Esrafili,et al. New route to 1,4-oxazepane and 1,4-diazepane derivatives: synthesis from N-propargylamines , 2016 .
[13] M. Esrafili,et al. New page to access pyridine derivatives: synthesis from N-propargylamines , 2016 .
[14] Yasuhiro Shiraishi,et al. Coumarin-Spiropyran Dyad with a Hydrogenated Pyran Moiety for Rapid, Selective, and Sensitive Fluorometric Detection of Cyanide Anion. , 2016, Analytical chemistry.
[15] M. Willis,et al. Homogeneous rhodium(i)-catalysis in de novo heterocycle syntheses. , 2016, Organic & biomolecular chemistry.
[16] M. Esrafili,et al. Novel routes to quinoline derivatives from N-propargylamines , 2016 .
[17] Hui Wang,et al. FeCl3-Mediated One-Pot Domino Reactions for the Synthesis of 9-Aryl/9-Arylethynyl-2,3,4,9-tetrahydro-1H-xanthen-1-ones from Propargylic Amines/Diaryl Amines and 1,3-Cyclohexanediones. , 2016, The Journal of organic chemistry.
[18] E. Vessally. A new avenue to the synthesis of highly substituted pyrroles: synthesis from N-propargylamines , 2016 .
[19] Mariana Macías-Alonso,et al. Coumarin heterocyclic derivatives: chemical synthesis and biological activity. , 2015, Natural product reports.
[20] R. Singla,et al. Coumarins as anticancer agents: a review on synthetic strategies, mechanism of action and SAR studies. , 2015, European journal of medicinal chemistry.
[21] Dattatraya H. Dethe,et al. FeCl3 mediated synthesis of substituted indenones by a formal [2+2] cycloaddition/ring opening cascade of o-keto-cinnamates. , 2015, Chemical communications.
[22] Jie Wang,et al. FeCl3-Mediated Synthesis of β-Alkynyl Ketones via Domino Nucleophilic-Substitution/Intramolecular-Cyclization/Reverse Claisen Condensation of N-Cyclohexyl Propargylamines and 1,3-Diketones. , 2015, The Journal of organic chemistry.
[23] H. Knölker,et al. Iron catalysis in organic synthesis. , 2015, Chemical reviews.
[24] Xinwei He,et al. Synthesis of coumarin-3-carboxylic esters via FeCl3-catalyzed multicomponent reaction of salicylaldehydes, Meldrum's acid and alcohols , 2015 .
[25] Qiannan Li,et al. Silver-mediated radical cyclization of alkynoates and α-keto acids leading to coumarins via cascade double C-C bond formation. , 2015, The Journal of organic chemistry.
[26] S. Ma,et al. Copper(I)-catalyzed three-component reaction of terminal propargyl alcohols, aldehydes, and amines: synthesis of 3-amino-2-pyrones and 2,5-dihydrofurans. , 2014, Angewandte Chemie.
[27] D. Back,et al. Iron(III) chloride and diorganyl diselenides-mediated 6-endo-dig cyclization of arylpropiolates and arylpropiolamides leading to 3-organoselenyl-2H-coumarins and 3-organoselenyl-quinolinones. , 2014, The Journal of organic chemistry.
[28] Q. Ding,et al. Copper-catalyzed direct trifluoromethylation of propiolates: construction of trifluoromethylated coumarins. , 2014, Organic letters.
[29] D. C. Deka,et al. Reaction of 6-aminouracils with aldehydes in water as both solvent and reactant under FeCl3·6H2O catalysis: towards 5-alkyl/arylidenebarbituric acids , 2014 .
[30] R. Weissleder,et al. Ultrafluorogenic coumarin-tetrazine probes for real-time biological imaging. , 2014, Angewandte Chemie.
[31] Zhuang-Ping Zhan,et al. Selective synthesis of 4-(sulfonyl)-methyl-1H-pyrazoles and (E)-4,5-dihydro-1H-pyrazoles from N-allenic sulfonylhydrazones. , 2014, Organic & biomolecular chemistry.
[32] Shi Jie,et al. An atom-economic synthesis of functionalized pyrroles via a sequential metal-catalyzed three-component reaction , 2014 .
[33] Xinwei He,et al. FeCl3-Catalyzed Cascade Reaction: An Efficient Approach to Functionalized Coumarin Derivatives , 2014 .
[34] D. Tejedor,et al. Coupled domino processes: synthesis of 3,5,8-trisubstituted coumarins from propargyl vinyl ethers. , 2013, The Journal of organic chemistry.
[35] Manman Sun,et al. FeCl3-catalyzed cascade cyclization in one pot: synthesis of ring-fused tetrahydroquinoline derivatives from arylamines and N-substituted lactams. , 2013, The Journal of organic chemistry.
[36] Michael F. Brown,et al. FeCl3 catalysed multicomponent divergent synthesis of a library of indeno-fused heterocycles , 2013 .
[37] P. Lu,et al. Three-component reaction of propargyl amines, sulfonyl azides, and alkynes: one-pot synthesis of tetrasubstituted imidazoles. , 2012, Organic letters.
[38] Lili Lin,et al. Completely OH-selective FeCl3-catalyzed Prins cyclization: highly stereoselective synthesis of 4-OH-tetrahydropyrans. , 2012, Journal of the American Chemical Society.
[39] Huimin Ma,et al. Spectroscopic probes with changeable π-conjugated systems. , 2012, Chemical communications.
[40] Chang-Hee Lee,et al. Synthesis of substituted coumarins via Brønsted acid mediated condensation of allenes with substituted phenols or anisoles. , 2012, The Journal of organic chemistry.
[41] Chin‐Fa Lee,et al. Synthesis of alkenyl sulfides through the iron-catalyzed cross-coupling reaction of vinyl halides with thiols. , 2012, The Journal of organic chemistry.
[42] Phil Ho Lee,et al. Iron(III)-catalyzed Conia-ene cyclization of 2-alkynic 1,3-dicarbonyl compounds. , 2012, The Journal of organic chemistry.
[43] Vsevolod A. Peshkov,et al. A walk around the A3-coupling. , 2012, Chemical Society reviews.
[44] Lei Wang,et al. Iron-promoted tandem reaction of anilines with styrene oxides via C-C cleavage for the synthesis of quinolines. , 2012, Organic letters.
[45] M. P. Yeh,et al. Facile synthesis of azaspirocycles via iron trichloride-promoted cyclization/chlorination of cyclic 8-aryl-5-aza-5-tosyl-2-en-7-yn-1-ols. , 2012, Organic letters.
[46] T. Hatakeyama,et al. Cross-coupling of non-activated chloroalkanes with aryl Grignard reagents in the presence of iron/N-heterocyclic carbene catalysts. , 2012, Organic letters.
[47] Zhiyong Wang,et al. One‐Pot Synthesis of 3,4‐Disubstituted Coumarins under Catalysis of Mn3O4 Nanoparticles , 2012 .
[48] K. S. Gupta,et al. Iron-catalyzed regioselective direct oxidative aryl-aryl cross-coupling. , 2011, The Journal of organic chemistry.
[49] Rajiv Karmakar,et al. A novel one pot route to flavones under dual catalysis, an organo- and a Lewis acid catalyst , 2011 .
[50] F. J. Fañanás,et al. Synthesis of 2,5-dihydropyridine derivatives by gold-catalyzed reactions of β-ketoesters and propargylamines. , 2011, Organic letters.
[51] Jaulang Hwang,et al. One-pot synthesis of luotonin A and its analogues. , 2011, Organic letters.
[52] Yeming Wang,et al. Iron-catalyzed synthesis of polysubstituted pyrroles via [4C+1N] cyclization of 4-acetylenic ketones with primary amines. , 2011, Chemical communications.
[53] F. Petitet,et al. Assessing the chemical diversity of an hsp90 database. , 2010, European journal of medicinal chemistry.
[54] U. Jana,et al. Iron(III)-catalyzed four-component coupling reaction of 1,3-dicarbonyl compounds, amines, aldehydes, and nitroalkanes: a simple and direct synthesis of functionalized pyrroles. , 2010, The Journal of organic chemistry.
[55] L. Albertazzi,et al. Polarity-sensitive coumarins tailored to live cell imaging. , 2010, Journal of the American Chemical Society.
[56] Zhiyong Wang,et al. Facile synthesis of sulfonyl amidines via carbon-nitrogen bond formation mediated by FeCl3. , 2009, Chemical communications.
[57] A. Padwa. Domino reactions of rhodium(II) carbenoids for alkaloid synthesis. , 2009, Chemical Society reviews.
[58] T. P. Lebold,et al. Zn(II)-Catalyzed synthesis of piperidines from propargyl amines and cyclopropanes. , 2009, Organic letters.
[59] J. Renoir,et al. Antiproliferative and apoptotic activities of tosylcyclonovobiocic acids as potent heat shock protein 90 inhibitors in human cancer cells. , 2009, Cancer letters.
[60] B. Wagner. The Use of Coumarins as Environmentally-Sensitive Fluorescent Probes of Heterogeneous Inclusion Systems , 2009, Molecules.
[61] Y. Takemoto,et al. Concise synthesis of the CDE ring system of tetrahydroisoquinoline alkaloids using carbophilic Lewis acid-catalyzed hydroamidation and oxidative Friedel-Crafts cyclization. , 2008, The Journal of organic chemistry.
[62] J. Renoir,et al. Synthesis and biological activity of simplified denoviose-coumarins related to novobiocin as potent inhibitors of heat-shock protein 90 (hsp90). , 2008, Bioorganic & medicinal chemistry letters.
[63] C. Bolm,et al. Iron-catalyzed S-arylation of thiols with aryl iodides. , 2008, Angewandte Chemie.
[64] C. Bolm,et al. Iron-catalyzed C-O cross-couplings of phenols with aryl iodides. , 2008, Angewandte Chemie.
[65] B. Stella,et al. New novobiocin analogues as antiproliferative agents in breast cancer cells and potential inhibitors of heat shock protein 90. , 2007, Journal of medicinal chemistry.
[66] Anthony Maxwell,et al. Novobiocin: redesigning a DNA gyrase inhibitor for selective inhibition of hsp90. , 2006, Journal of the American Chemical Society.
[67] H. Rao,et al. Condensation of alpha-aroylketene dithioacetals and 2-hydroxyarylaldehydes results in facile synthesis of a combinatorial library of 3-aroylcoumarins. , 2006, The Journal of organic chemistry.
[68] Chao-Hsiung Lin,et al. Recent advances in coumarins and 1-azacoumarins as versatile biodynamic agents. , 2006, Current medicinal chemistry.
[69] J. Du Bois,et al. A synthesis of (+)-saxitoxin. , 2006, Journal of the American Chemical Society.
[70] Lourdes Santana,et al. A QSAR model for in silico screening of MAO-A inhibitors. Prediction, synthesis, and biological assay of novel coumarins. , 2006, Journal of medicinal chemistry.
[71] H. Alper,et al. An efficient synthesis of propargylamines via C-H activation catalyzed by copper(I) in ionic liquids. , 2005, Chemical communications.
[72] G. Baronetti,et al. A solvent-free synthesis of coumarins using a Wells-Dawson heteropolyacid as catalyst , 2004 .
[73] D. Hadjipavlou-Litina,et al. Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities. , 2004, Current pharmaceutical design.
[74] H. Katerinopoulos. The coumarin moiety as chromophore of fluorescent ion indicators in biological systems. , 2004, Current pharmaceutical design.
[75] C. Garbay,et al. A very short route to enantiomerically pure coumarin-bearing fluorescent amino acids. , 2004, Angewandte Chemie.
[76] B. Jiang,et al. Highly enantioselective construction of fused pyrrolidine systems that contain a quaternary stereocenter: concise formal synthesis of (+)-conessine. , 2004, Angewandte Chemie.
[77] Y. Tu,et al. Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water. , 2004, Organic letters.
[78] K. Lee,et al. Recent progress in the development of coumarin derivatives as potent anti‐HIV agents , 2003, Medicinal research reviews.
[79] B. Trost,et al. Atom economy. Palladium-catalyzed formation of coumarins by addition of phenols and alkynoates via a net C-H insertion. , 2003, Journal of the American Chemical Society.
[80] G. Fabrizi,et al. Preparation of 2,5-disubstituted oxazoles from N-propargylamides. , 2001, Organic letters.
[81] Koichi Tanaka,et al. Solvent-Free Coumarin Synthesis , 2001 .
[82] L. Neckers,et al. Novobiocin and related coumarins and depletion of heat shock protein 90-dependent signaling proteins. , 2000, Journal of the National Cancer Institute.
[83] S. Nishibe,et al. Coumarins, the bioactive structures with antifungal property , 2000 .
[84] S. Farid,et al. Ketocoumarins: A new class of triplet sensitizers , 1982 .
[85] E. Knoevenagel,et al. 692. Condensationen von Salicylaldehyd mit Cyanessigester, Benzoylessigester und Acetylaceton , 1904 .