Literature DB >> 19813765

InBr3: a versatile catalyst for the different types of Friedel-Crafts reactions.

Ponnaboina Thirupathi1, Sung Soo Kim.   

Abstract

Mild and efficient InBr(3)-catalyzed Friedel-Crafts alkylation of heteroaromatic or electron-rich aromatic compounds with alpha-amido sulfones at room temperature in CH(2)Cl(2) has been developed. The products undergo further Friedel-Crafts alkylation with heteroaromatic or electron-rich aromatic compounds leading to unsymmetrical or bis-symmetrical triaryl methanes in good yield. Alpha-amido sulfones are employed for the synthesis of the unsymmetrical and bis-symmetrical triaryl methanes. The use of mild reaction condition, low catalytic loading, and high yield are the advantages of the present procedures.

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Year:  2009        PMID: 19813765     DOI: 10.1021/jo9014613

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Using In(III) as a promoter for glycosylation.

Authors:  Amanda L Mattson; Anna K Michel; Mary J Cloninger
Journal:  Carbohydr Res       Date:  2011-10-17       Impact factor: 2.104

2.  Metal- and solvent-free synthesis of aniline- and phenol-based triarylmethanes via Brönsted acidic ionic liquid catalyzed Friedel-Crafts reaction.

Authors:  Nipaphorn Ponpao; Warapong Senapak; Rungnapha Saeeng; Jaray Jaratjaroonphong; Uthaiwan Sirion
Journal:  RSC Adv       Date:  2021-06-30       Impact factor: 4.036

3.  1-(N-Acylamino)alkyltriarylphosphonium Salts with Weakened Cα-P⁺ Bond Strength-Synthetic Applications.

Authors:  Jakub Adamek; Anna Węgrzyk; Justyna Kończewicz; Krzysztof Walczak; Karol Erfurt
Journal:  Molecules       Date:  2018-09-25       Impact factor: 4.411

  3 in total

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