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- W107780867 endingPage "141" @default.
- W107780867 startingPage "115" @default.
- W107780867 abstract "Alkylation reactions utilizing nontoxic Lewis acid catalysts and green alkylating reagents are of high interest due to the continuous need for environmentally benign C-C and C-X bond formation. This article shows recent advances in Bi(III)-catalyzed alkylations of arenes, 2,4-pentanediones and various oxygen- and nitrogen-containing nucleophiles. Instead of toxic alkyl halides, the electrophilic components for these transformations were benzyl and propargyl alcohols as well as substrates with activated double bonds such as styrenes. The fact that Bi(III) salts are capable of activating both σ- and π-donors highlights their unique character as versatile catalysts for catalytic alkylation reactions. In addition, Bi(III) salts are less toxic and cheaper than other Lewis acids that have been described for similar transformations." @default.
- W107780867 created "2016-06-24" @default.
- W107780867 creator A5071153001 @default.
- W107780867 creator A5084678547 @default.
- W107780867 date "2011-01-01" @default.
- W107780867 modified "2023-09-24" @default.
- W107780867 title "Bismuth Salts in Catalytic Alkylation Reactions" @default.
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- W107780867 doi "https://doi.org/10.1007/128_2011_191" @default.
- W107780867 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21728137" @default.
- W107780867 hasPublicationYear "2011" @default.
- W107780867 type Work @default.