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Heteroarenes overview

This overview impressively demonstrates that Bi(III) salts are not only versatile Lewis acid catalysts for the activation of cr-donors, including benzyl and propargyl alcohols, but also efficient catalysts for the activation of Ji-donors such as styrenes or alkynes. In recent years, various environmentally benign bismuth-catalyzed methods have been developed for the alkylation of arenes, heteroarenes,... [Pg.139]

The Minisci reaction has successfully been applied for the alkylation of various heteroarenes, i. e. lepidine, pyrazine, quinoline and quinoxaline [2e, 2g, 10]. Organic compounds such as alkanes, alkenes, carboxylic acids, esters, amides, amines, alcohols, ethers, aldehydes, ketones, halides etc. have been successfully used as radical precursors in the Minisci reaction. A good overview of the different methods which have been applied to generate the alkyl radicals in these processes is summarized in [10b]. [Pg.565]


See other pages where Heteroarenes overview is mentioned: [Pg.1004]    [Pg.140]    [Pg.223]    [Pg.676]    [Pg.309]   
See also in sourсe #XX -- [ Pg.648 ]




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Heteroarene

Heteroarenes

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