Literature DB >> 22565609

Synthesis of amino-substituted indoles using the Bartoli reaction.

Laura Wylie1, Paolo Innocenti, Daniel K Whelligan, Swen Hoelder.   

Abstract

We report herein the concise preparation of a range of functionalised aminoindoles via a new application of the Bartoli reaction. Scope and limitations of the methodology have been extensively studied to reveal the importance of protecting groups and substitution patterns. The use of amino substituted nitroanilines for the Bartoli reaction is to our knowledge unprecedented. Our work thus represents a novel entry into substituted aminoindoles which are relevant building blocks for both the fine chemical and pharmaceutical industry.

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Year:  2012        PMID: 22565609     DOI: 10.1039/c2ob25256b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  A palladium-catalyzed Barluenga cross-coupling - reductive cyclization sequence to substituted indoles.

Authors:  S M Ashikur Rahman; Björn C G Söderberg
Journal:  Tetrahedron       Date:  2021-07-06       Impact factor: 2.388

  1 in total

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