cheminform abstract: palladium-catalyzed cross-coupling reactions of 1,2-diiodoalkenes with terminal...

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ChemInform 2009, 40, issue 17 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Alkynes Q 0087 Palladium-Catalyzed Cross-Coupling Reactions of 1,2-Diiodoalkenes with Termi- nal Alkynes: Selective Synthesis of Unsymmetrical Buta-1,3-diynes and 2-Ethy- nylbenzofurans. — A novel approach for the highly selective synthesis of unsymmet- rical diynes is developed through Pd-catalyzed coupling/elimination of terminal al- kynes with (E)-1,2-diiodoalkynes. When o-hydroxyalkynes are used, 2-ethynylbenzo- furans can be synthesized by simple heating after diyne formation. — (LIANG, Y.; TAO, L.-M.; ZHANG, Y.-H.; LI*, J.-H.; Synthesis 2008, 24, 3988-3994; Key Lab. Chem. Biol., Hunan Norm. Univ., Changsha, Hunan 410081, Peop. Rep. China; Eng.) — Mais 17- 070

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www.cheminform.wiley-vch.de

AlkynesQ 0087 Palladium-Catalyzed Cross-Coupling Reactions of 1,2-Diiodoalkenes with Termi-

nal Alkynes: Selective Synthesis of Unsymmetrical Buta-1,3-diynes and 2-Ethy-nylbenzofurans. — A novel approach for the highly selective synthesis of unsymmet-rical diynes is developed through Pd-catalyzed coupling/elimination of terminal al-kynes with (E)-1,2-diiodoalkynes. When o-hydroxyalkynes are used, 2-ethynylbenzo-furans can be synthesized by simple heating after diyne formation. — (LIANG, Y.; TAO, L.-M.; ZHANG, Y.-H.; LI*, J.-H.; Synthesis 2008, 24, 3988-3994; Key Lab. Chem. Biol., Hunan Norm. Univ., Changsha, Hunan 410081, Peop. Rep. China; Eng.) — Mais

17- 070

ChemInform 2009, 40, issue 17 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim