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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 26, 1996 - Issue 18
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Original Articles

Oxidative Addition of 4-Hydroxycoumarin to Alkenes. An Expeditious Entry to 2,3-Dihydro-4H-furo-[3,2-c][1]benzopyran-4-ones1

Giovanni Appendino Dipartimento di Scienza e Tecnologia del Farmaco, Via Giuria 9, 10125, Torino, Italy
,
Giancarlo Cravotto Dipartimento di Scienza e Tecnologia del Farmaco, Via Giuria 9, 10125, Torino, Italy
,
Giovanni Palmisano Dipartimento di Scienza e Tecnologia del Farmaco, Via Giuria 9, 10125, Torino, Italy
&
Rita Annunziata Dipartimento di Chimica Organica e Industriale, Via Venezian 21, 20133, Milano, Italy
Pages 3359-3371 | Received 11 Mar 1996, Published online: 21 Aug 2006

Citations (15)

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Mehmet Yılmaz, Mehtap Yakut & A. Tarık Pekel. (2008) Synthesis of 2,3‐Dihydro‐4H‐furo[3,2‐c] chromen‐4‐ones and 2,3‐Dihydronaphtho[2,3‐b]furan‐4,9‐diones by the Radical Cyclizations of Hydroxyenones with Electron-Rich Alkenes using Manganese(III) Acetate. Synthetic Communications 38:6, pages 914-927.
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Gregory Bar, Fabien Bini & Andrew F. Parsons. (2003) CAN-Mediated Oxidative Free Radical Reactions in an Ionic Liquid. Synthetic Communications 33:2, pages 213-222.
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Articles from other publishers (13)

Rui Chang, Yubing Pang & Juntao Ye. (2023) Divergent Photosensitizer Controlled Reactions of 4‐Hydroxycoumarins and Unactivated Olefins: Hydroarylation and Subsequent [2+2] Cycloaddition. Angewandte Chemie International Edition 62:45.
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Rui Chang, Yubing Pang & Juntao Ye. (2023) Divergent Photosensitizer Controlled Reactions of 4‐Hydroxycoumarins and Unactivated Olefins: Hydroarylation and Subsequent [2+2] Cycloaddition. Angewandte Chemie.
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Iván Cortés, L. Javier Cala, Andrea B. J. Bracca & Teodoro S. Kaufman. (2020) Furo[3,2- c ]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms . RSC Advances 10:55, pages 33344-33377.
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Chuang Qiao, Wen Zhang, Jing-Chun Han & Chuang-Chuang Li. (2016) Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic Letters 18:19, pages 4932-4935.
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Yafei Yuan, Yu Feng, Fengxia Ren, Shubin Niu, Xingzhong Liu & Yongsheng Che. (2013) A Botryane Metabolite with a New Hexacyclic Skeleton from an Entomogenous Fungus Hypocrea sp. . Organic Letters 15:23, pages 6050-6053.
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Jonathan W. Burton. 2012. Encyclopedia of Radicals in Chemistry, Biology and Materials. Encyclopedia of Radicals in Chemistry, Biology and Materials.
Mehmet Yılmaz. (2011) Studies on the Radical Cyclization of 3‐Oxopropanenitriles and Alkenes with Cerium(IV) Ammonium Nitrate in Ether Solvents. Helvetica Chimica Acta 94:7, pages 1335-1342.
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A.J. Phillips, J.A. Henderson & K.L. Jackson. 2008. Comprehensive Heterocyclic Chemistry III. Comprehensive Heterocyclic Chemistry III 337 418 .
Ronald Grigg, Mohammad Nurnabi & M.Ruhul A Sarkar. (2004) Dihydrofurocoumarin and dihydrofurodihydropyrid-2-one derivatives via palladium catalysed cascades involving aryl/heteroaryl/vinyl iodides and allene followed by acid catalysed cyclisation. Tetrahedron 60:15, pages 3359-3373.
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Francesco Risitano, Giovanni Grassi, Francesco Foti & Cristina Bilardo. (2001) A convenient synthesis of furo[3,2-c]coumarins by a tandem alkylation/intramolecular aldolisation reaction. Tetrahedron Letters 42:20, pages 3503-3505.
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Giovanni Appendino, Giancarlo Cravotto, Giovanni B. Giovenzana & Giovanni Palmisano. (1999) A Straightforward Entry into Polyketide Monoprenylated Furanocoumarins and Pyranocoumarins. Journal of Natural Products 62:12, pages 1627-1631.
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Sergio Cenini, Giancarlo Cravotto, Giovanni B. Giovenzana, Giovanni Palmisano & Stefano Tollari. (1999) Polyoxygenated coumarins. Oxonium ylides en route to polyoxa-macrocyclic coumarins. Tetrahedron 55:21, pages 6577-6584.
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G. APPENDINO, G. CRAVOTTO, G. PALMISANO & R. ANNUNZIATA. (2010) ChemInform Abstract: The Chemistry of Coumarin Derivatives. Part 8. Oxidative Addition of 4‐ Hydroxycoumarin to Alkenes. An Expeditious Entry to 2,3‐Dihydro‐4H‐ furo(3,2‐c)(1)benzopyran‐4‐ones.. ChemInform 27:49.
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