Pure and Applied Chemistry

CrossRef Cited-by Linking

• Walleser Patrick, Brückner Reinhard: Stereocontrolled Synthesis of a C1 -C10 Building Block (“Southwestern Moiety”) for the Unnatural Enantiomers of the Polyene Polyol Antibiotics Filipin III and Pentamycin: A Sultone-Forming Ring-Closing Metathesis for Protection of Homoallylic Alcohols. Eur. J. Org. Chem. 2014, n/a. <http://dx.doi.org/10.1002/ejoc.201400145>
• Kamptmann Sonja B., Brückner Reinhard: Stereocontrolled Synthesis of a C n -C n +7 Building Block (“Eastern Moiety”) for the Unnatural Enantiomers of Important Polyol,Polyene Antibiotics Based on a Ring-Closing Metathesis and an Aldol Addition of a Lactone Enolate. Eur. J. Org. Chem. 2013, 2013, 6584. <http://dx.doi.org/10.1002/ejoc.201300183>
• Huang Jinhua, Yang Jessica R., Zhang Jin, Yang Jiong: Total synthesis and structure–activity relationship study of the potent cAMP signaling agonist (−)-alotaketal A. Org. Biomol. Chem. 2013, 11, 3212. <http://dx.doi.org/10.1039/c3ob40120k>
• Goel Atul, Taneja Gaurav, Raghuvanshi Ashutosh, Kant Ruchir, Maulik Prakas R.: Diversity-oriented general protocol for the synthesis of privileged oxygen scaffolds: pyrones, coumarins, benzocoumarins and naphthocoumarins. Org. Biomol. Chem. 2013, 11, 5239. <http://dx.doi.org/10.1039/c3ob40859k>
• Oberholzer Miriam, Gerber Roman, Frech Christian M.: Mizoroki-Heck Reactions Catalyzed by Dichloro{bis[1-(dicyclohexylphosphanyl)piperidine]}palladium: Palladium Nanoparticle Formation Promoted by (Water-Induced) Ligand Degradation. Synth Catal 2012, 354, 627. <http://dx.doi.org/10.1002/adsc.201100646>
• Hon Yung-Son, Hong Ya-Chun, Hong Bor-Cherng, Liao Ju-Hsiou: The First Synthesis of Natural Occurring Juncaceae Coumarin, 9-Hydroxy-8-methyl-3H-benzo[f]chromen-3-one, Featuring a One-pot Rearrangement and Aromatization Cascade. Jnl Chinese Chemical Soc 2012, 59, 407. <http://dx.doi.org/10.1002/jccs.201100481>
• Beletskaya I. P., Fedorov A. Yu., Nyuchev A. V.: Catalytic methods of creation and functionalization of the coumarin skeleton. Chem Heterocycl Compd 2012, 48, 166. <http://dx.doi.org/10.1007/s10593-012-0980-8>
• Kim Sundae, Kang Dongjin, Lee Chang-Hee, Lee Phil Ho: Synthesis of Substituted Coumarins via Brønsted Acid Mediated Condensation of Allenes with Substituted Phenols or Anisoles. J. Org. Chem. 2012, 77, 6530. <http://dx.doi.org/10.1021/jo301086k>
• Ferguson Jamie, Zeng Fanlong, Alper Howard: Synthesis of Coumarins via Pd-Catalyzed Oxidative Cyclocarbonylation of 2-Vinylphenols. Org. Lett. 2012, 14, 5602. <http://dx.doi.org/10.1021/ol302725x>
• Martin Tioga J., Vakhshori Venus G., Tran Yang S., Kwon Ohyun: Phosphine-Catalyzed β′-Umpolung Addition of Nucleophiles to Activated α-Alkyl Allenes. Org Lett 2011, 13, 2586. <http://dx.doi.org/10.1021/ol200697m>
• Schmidt Bernd, Krehl Stefan: A single precatalyst tandem RCM–allylic oxidation sequence. Chem Commun 2011, 47, 5879. <http://dx.doi.org/10.1039/c1cc11347j>
• Rao Maddali L. N., Venkatesh Varadhachari, Jadhav Deepak N.: Palladium-Catalyzed Synthesis of 4-Arylcoumarins Using Triarylbismuth Compounds as Atom-Efficient Multicoupling Organometallic Nucleophiles. Eur J Org Chem 2010, 2010, 3945. <http://dx.doi.org/10.1002/ejoc.201000134>
• Giguère Denis, Patnam Ramesh, Juarez-Ruiz Juan M., Neault Mathieu, Roy René: Catalytic synthesis of novel 4-C-glycosyl coumarins using a domino Heck reaction/lactonization process. Tetrahetron Lett 2009, 50, 4254. <http://dx.doi.org/10.1016/j.tetlet.2009.04.134>
• C. Majumdar Krishna, Muhuri Sanjukta, Ul Islam Rafique, Chattopadhyay Buddhadeb: Synthesis of Five- and Six-Membered Heterocyclic Compounds by the Application of the Metathesis Reactions. HETEROCYCLES 2009, 78, 1109. <http://dx.doi.org/10.3987/REV-08-646>
• Brass Sascha, Chan Nan-Si, Gerlach Christof, Luksch Torsten, Böttcher Jark, Diederich Wibke E.: Synthesis of 2,3,4,7-tetrahydro-1H-azepines as privileged ligand scaffolds for the design of aspartic protease inhibitors via a ring-closing metathesis approach. J Organomet Chem 2006, 691, 5406. <http://dx.doi.org/10.1016/j.jorganchem.2006.09.031>
• Oyamada Juzo, Kitamura Tsugio: Synthesis of coumarins by Pt-catalyzed hydroarylation of propiolic acids with phenols. Tetrahedron 2006, 62, 6918. <http://dx.doi.org/10.1016/j.tet.2006.04.080>
• Liu Yannan, Mills Aaron D., Kurth Mark J.: Solid phase synthesis of 3-(5-arylpyridin-2-yl)-4-hydroxycoumarins. Tetrahetron Lett 2006, 47, 1985. <http://dx.doi.org/10.1016/j.tetlet.2006.01.069>
• Polito Laura, Cravini Massimiliano, Poletti Laura, Lay Luigi: Simple Synthesis of Versatile Coumarin Scaffolds. Synth Comm 2006, 36, 2203. <http://dx.doi.org/10.1080/00397910600638937>
• Battistuzzi Gianfranco, Cacchi Sandro, De Salve Ilse, Fabrizi Giancarlo, Parisi Luca M.: Synthesis of Coumarins in a Moltenn-Bu4NOAc/n-Bu4NBr Mixture through a Domino Heck Reaction/Cyclization Process. Adv Synth Catal 2005, 347, 308. <http://dx.doi.org/10.1002/adsc.200404297>
• Nosse Bernd, Schall Andreas, Jeong Won Boo, Reiser Oliver: Optimization of Ring-Closing Metathesis: Inert Gas Sparging and Microwave Irradiation. Adv Synth Catal 2005, 347, 1869. <http://dx.doi.org/10.1002/adsc.200505137>
• Herndon James W.: The chemistry of the carbon-transition metal double and triple bond: annual survey covering the year 2003. Coord Chem Rev - 2005, 249, 999. <http://dx.doi.org/10.1016/j.ccr.2004.10.009>
• Sharma G.V.M., Janardhan Reddy J., Sree Lakshmi P., Radha Krishna P.: An efficient ZrCl4 catalyzed one-pot solvent free protocol for the synthesis of 4-substituted coumarins. Tetrahetron Lett 2005, 46, 6119. <http://dx.doi.org/10.1016/j.tetlet.2005.06.166>
• Grubbs Robert H.: Olefin metathesis. Tetrahedron 2004, 60, 7117. <http://dx.doi.org/10.1016/j.tet.2004.05.124>
• Zhu Lei, Lynch Vincent M., Anslyn Eric V.: FRET induced by an ‘allosteric’ cycloaddition reaction regulated with exogenous inhibitor and effectors. Tetrahedron 2004, 60, 7267. <http://dx.doi.org/10.1016/j.tet.2004.06.079>
• Perron Julien, Joseph Benoît, Mérour Jean-Yves: Access to ring-fused azepino[3,4-b]indole-1,5-dione derivatives by ring-closing olefin metathesis. Tetrahedron 2004, 60, 10099. <http://dx.doi.org/10.1016/j.tet.2004.07.069>