Literature DB >> 29161050

FeCl3-Mediated Domino Reaction of Benzoxazinones with Aroylmethylidene Malonates: Synthesis to Functionalized Pyrrolobenzoxazines.

Shweta Bisht1, Rama Krishna Peddinti1.   

Abstract

An efficient domino approach for the synthesis of pyrrolobenzoxazine derivatives is described. The FeCl3-promoted domino reaction between aroylmethylidene malonates and benzoxazinones has been successfully established to afford the title compounds in good to excellent yield under mild reaction conditions. The domino protocol provides a concise and straightforward access to highly substituted pyrrolobenzoxazines with high efficiency and excellent functional group tolerance.

Entities:  

Year:  2017        PMID: 29161050     DOI: 10.1021/acs.joc.7b02207

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


  3 in total

1.  Synthesis of indole-cycloalkyl[b]pyridine hybrids via a four-component six-step tandem process.

Authors:  Muthumani Muthu; Rakkappan Vishnu Priya; Abdulrahman I Almansour; Raju Suresh Kumar; Raju Ranjith Kumar
Journal:  Beilstein J Org Chem       Date:  2018-11-22       Impact factor: 2.883

2.  Biocatalytic decarboxylative Michael addition for synthesis of 1,4-benzoxazinone derivatives.

Authors:  Hossein Bavandi; Mansour Shahedi; Zohreh Habibi; Maryam Yousefi; Jesper Brask; Mehdi Mohammadi
Journal:  Sci Rep       Date:  2022-07-26       Impact factor: 4.996

3.  Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol.

Authors:  Ekaterina E Stepanova; Maksim V Dmitriev; Andrey N Maslivets
Journal:  Beilstein J Org Chem       Date:  2020-09-21       Impact factor: 2.883

  3 in total

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