An efficient synthesis of 4-substituted coumarin derivatives via a palladium-catalyzed Suzuki cross-coupling reaction

[1]  F. Rominger,et al.  Synthesis of functionalized chromones through sequential reactions in aqueous media. , 2014, Organic & biomolecular chemistry.

[2]  Kenneth S Hettie,et al.  ExoSensor 517: a dual-analyte fluorescent chemosensor for visualizing neurotransmitter exocytosis. , 2013, ACS chemical neuroscience.

[3]  Shikha Sharma,et al.  Experimental and computational studies on the [3,3]- and [3,5]-sigmatropic rearrangements of acetoxycyclohexadienones: a non-ionic mechanism for acyl migration. , 2013, Journal of the American Chemical Society.

[4]  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.

[5]  Abbas Shafiee,et al.  A facile route to flavone and neoflavone backbones via a regioselective palladium catalyzed oxidative Heck reaction. , 2012, Chemical communications.

[6]  Ding-Yah Yang,et al.  One-pot synthesis of pyranocoumarins via microwave-assisted pseudo multicomponent reactions and their molecular switching properties. , 2012, Organic letters.

[7]  Xinmei Fu,et al.  Palladium-catalyzed oxidative Heck coupling reaction for direct synthesis of 4-arylcoumarins using coumarins and arylboronic acids. , 2012, The Journal of organic chemistry.

[8]  R. Rieke,et al.  A novel organozinc reagent 4-coumarinylzinc bromide; preparation and application in the synthesis of 4-substituted coumarin derivatives , 2011 .

[9]  C. Shayo,et al.  Coumarins: old compounds with novel promising therapeutic perspectives. , 2010, Current medicinal chemistry.

[10]  S. Ham,et al.  Multiphoton infrared initiated thermal reactions of esters: pseudopericyclic eight-centered cis-elimination. , 2009, Journal of the American Chemical Society.

[11]  J. Genêt,et al.  Potassium organotrifluoroborates: new perspectives in organic synthesis. , 2008, Chemical reviews.

[12]  G. Molander,et al.  Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction. , 2007, Accounts of chemical research.

[13]  G. Molander,et al.  Suzuki-Miyaura cross-coupling reactions of benzyl halides with potassium aryltrifluoroborates. , 2006, The Journal of organic chemistry.

[14]  I. Beletskaya,et al.  Synthesis of 4-heteroaryl-substituted coumarins by Suzuki cross-coupling reactions , 2004 .

[15]  D. Hadjipavlou-Litina,et al.  Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities. , 2004, Current pharmaceutical design.

[16]  R. O’Kennedy,et al.  Studies on coumarins and coumarin-related compounds to determine their therapeutic role in the treatment of cancer. , 2004, Current pharmaceutical design.

[17]  V. Khilya,et al.  Neoflavones. 1. Natural Distribution and Spectral and Biological Properties , 2004, Chemistry of Natural Compounds.

[18]  M. H. Babu,et al.  The indium(III) chloride-catalyzed von Pechmann reaction: a simple and effective procedure for the synthesis of 4-substituted coumarins , 2002 .

[19]  G. Molander,et al.  Suzuki-Miyaura cross-coupling reactions of potassium alkenyltrifluoroborates. , 2002, The Journal of organic chemistry.

[20]  M. Rivero,et al.  Suzuki cross-coupling reactions of potassium alkenyltrifluoroborates. , 2002 .

[21]  Y. Liao,et al.  Synthesis of 4-substituted coumarins via the palladium-catalyzed cross-couplings of 4-tosylcoumarins with terminal acetylenes and organozinc reagents. , 2001, The Journal of organic chemistry.

[22]  Arthur T. Andrews,et al.  Activation of Aryl Chlorides for Suzuki Cross-Coupling by Ligandless, Heterogeneous Palladium , 2001 .

[23]  S. Ham,et al.  [1,3], [3,3], and [3,5] Sigmatropic Rearrangements of Esters Are Pseudopericyclic , 1999 .

[24]  D. Donnelly,et al.  Synthesis of neoflavones by Suzuki arylation of 4-substituted coumarins , 1996 .

[25]  D. Donnelly,et al.  Isoflavonoids and neoflavonoids: naturally occurring O-heterocycles , 1995 .

[26]  L. Overman.  A general method for the synthesis of amines by the rearrangement of allylic trichloroacetimidates. 1,3 Transposition of alcohol and amine functions , 1976 .