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ChemInform 2011, 42, issue 45 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Polyphenylalkene derivatives Q 0740 DOI: 10.1002/chin.201145081 Selenoether Ligand Assisted Heck Catalysis. — The reaction of aryl bromides with butyl acrylate or styrene is catalyzed effectively by the catalyst, generated in situ from (I) and PdCl2, or by the pre-made catalysts (II) or (III). The reaction conditions are not suitable for aryl chlorides. Addition of Bu4NBr allows the preparation of (VI) from 4-chloroacetophenone (VII), albeit with low yields. — (CHAKRABORTY, T.; SRIVASTAVA, K.; SINGH*, H. B.; BUTCHER, R. J.; J. Organomet. Chem. 696 (2011) 13, 2559-2564, http://dx.doi.org/10.1016/j.jorganchem.2011.03.047 ; Dep. Chem., Indian Inst. Technol., Mumbai 400 076, India; Eng.) — Y. Steudel 45- 081

ChemInform Abstract: Selenoether Ligand Assisted Heck Catalysis

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Polyphenylalkene derivativesQ 0740 DOI: 10.1002/chin.201145081

Selenoether Ligand Assisted Heck Catalysis. — The reaction of aryl bromides with butyl acrylate or styrene is catalyzed effectively by the catalyst, generated in situ from (I) and PdCl2, or by the pre-made catalysts (II) or (III). The reaction conditions are not suitable for aryl chlorides. Addition of Bu4NBr allows the preparation of (VI) from 4-chloroacetophenone (VII), albeit with low yields. — (CHAKRABORTY, T.; SRIVASTAVA, K.; SINGH*, H. B.; BUTCHER, R. J.; J. Organomet. Chem. 696 (2011) 13, 2559-2564, http://dx.doi.org/10.1016/j.jorganchem.2011.03.047 ; Dep. Chem., Indian Inst. Technol., Mumbai 400 076, India; Eng.) — Y. Steudel

45- 081

ChemInform 2011, 42, issue 45 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim