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ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Ketones Q 0350 DOI: 10.1002/chin.201236061 Iridium Catalyzed Chemoselective Alkylation of 2'-Aminoacetophenone with Primary Benzyl Type Alcohols under Microwave Conditions. — The direction of the iridium-catalyzed alkylation of 2'-aminoacetophenone (I) with benzyl alcohols (II) depends on the reaction conditions leading either to C-alkylated products (III) or to N-alkylated derivatives (IV). — (BHAT, S.; SRIDHARAN*, V.; Chem. Commun. (Cambridge) 48 (2012) 39, 4701-4703, http://dx.doi.org/10.1039/c2cc31055d ; Sch. Chem., Univ. Leeds, Leeds LS2 9JT, UK; Eng.) — R. Staver 36- 061

ChemInform Abstract: Iridium Catalyzed Chemoselective Alkylation of 2′-Aminoacetophenone with Primary Benzyl Type Alcohols under Microwave Conditions

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Page 1: ChemInform Abstract: Iridium Catalyzed Chemoselective Alkylation of 2′-Aminoacetophenone with Primary Benzyl Type Alcohols under Microwave Conditions

KetonesQ 0350 DOI: 10.1002/chin.201236061

Iridium Catalyzed Chemoselective Alkylation of 2'-Aminoacetophenone with Primary Benzyl Type Alcohols under Microwave Conditions. — The direction of the iridium-catalyzed alkylation of 2'-aminoacetophenone (I) with benzyl alcohols (II) depends on the reaction conditions leading either to C-alkylated products (III) or to N-alkylated derivatives (IV). — (BHAT, S.; SRIDHARAN*, V.; Chem. Commun. (Cambridge) 48 (2012) 39, 4701-4703, http://dx.doi.org/10.1039/c2cc31055d ; Sch. Chem., Univ. Leeds, Leeds LS2 9JT, UK; Eng.) — R. Staver

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ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim