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Collect. Czech. Chem. Commun. 2006, 71, 667-678

Intensification of a Reaction by the Addition of a Minor Amount of Solvent: Diels-Alder Reaction of 2H-Pyran-2-ones with Alkynes

Krištof Kranjc and Marijan Kočevar*

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Aškerčeva 5, SI-1000 Ljubljana, Slovenia

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  • Heravi Majid M., Dehghani Mahzad, Zadsirjan Vahideh, Ghanbarian Manijheh: Alkynes as Privileged Synthons in Selected Organic Name Reactions. COS 2019, 16, 205. <>
  • Smith Laura K., Baxendale Ian R.: Flow synthesis of coumalic acid and its derivatization. React. Chem. Eng. 2018, 3, 722. <>
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  • Kappe C. Oliver, Dallinger Doris: Controlled microwave heating in modern organic synthesis: highlights from the 2004–2008 literature. Mol Divers 2009, 13, 71. <>
  • Kranjc Krištof, Kočevar Marijan: An expedient route to indoles via a cycloaddition/cyclization sequence from (Z)-1-methoxybut-1-en-3-yne and 2H-pyran-2-ones. Tetrahedron 2008, 64, 45. <>
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  • Kranjc Krištof, Kocevar Marijan: Enhancing a Neat Microwave-Assisted Transformation. Diels–Alder Reaction of 2H-Pyran-2-ones toward Fused Bicyclo[2.2.2]octenes. BCSJ 2007, 80, 2001. <>
  • Kočevar Marijan, Hren Jure, Kranjc Kristof, Polanc Slovenko: Bicyclo[2.2.2]oct-7-ene Derivatives: A Green Preparation of the Fused Succinimide Ring. HETEROCYCLES 2007, 72, 399. <>
  • Kranjc Kristof, Kocevar Marijan: Intensification of a Reaction by the Addition of a Minor Amount of Solvent: Diels—Alder Reaction of 2H-Pyran-2-ones with Alkynes. ChemInform 2006, 37. <>