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ChemInform 2011, 42, issue 39 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Polyphenylalkane derivatives Q 0720 DOI: 10.1002/chin.201139064 Palladium-Catalyzed Decarboxylative Arylation of Potassium Cyanoacetate: Synthesis of α-Diaryl Nitriles from Aryl Halides. — In most cases, potassium cy- anoacetate (I) produces higher yields than its sodium analogue (VIII). If phenol-derived electrophiles (IVc) and (IVd) are used, the base-sensitive triflate produces a good, whereas arylation with the tosylate fails. — (YEUNG, P. Y.; CHUNG, K. H.; KWONG*, F. Y.; Org. Lett. 13 (2011) 11, 2912-2915, http://dx.doi.org/10.1021/ol2009522 ; Dep. Appl. Biol. Chem. Technol., Hong Kong Polytech. Univ., Hung Hom, Hong Kong, Peop. Rep. China; Eng.) — H. Simon 39- 064

ChemInform Abstract: Palladium-Catalyzed Decarboxylative Arylation of Potassium Cyanoacetate: Synthesis of α-Diaryl Nitriles from Aryl Halides

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Polyphenylalkane derivativesQ 0720 DOI: 10.1002/chin.201139064

Palladium-Catalyzed Decarboxylative Arylation of Potassium Cyanoacetate: Synthesis of α-Diaryl Nitriles from Aryl Halides. — In most cases, potassium cy-anoacetate (I) produces higher yields than its sodium analogue (VIII). If phenol-derived electrophiles (IVc) and (IVd) are used, the base-sensitive triflate produces a good, whereas arylation with the tosylate fails. — (YEUNG, P. Y.; CHUNG, K. H.; KWONG*, F. Y.; Org. Lett. 13 (2011) 11, 2912-2915, http://dx.doi.org/10.1021/ol2009522 ; Dep. Appl. Biol. Chem. Technol., Hong Kong Polytech. Univ., Hung Hom, Hong Kong, Peop. Rep. China; Eng.) — H. Simon

39- 064

ChemInform 2011, 42, issue 39 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim