Literature DB >> 24357122

An advanced and novel one-pot synthetic method for diverse benzo[c]chromen-6-ones by transition-metal free mild base-promoted domino reactions of substituted 2-hydroxychalcones with β-ketoesters and its application to polysubstituted terphenyls.

Tej Narayan Poudel1, Yong Rok Lee.   

Abstract

Novel and efficient one-pot syntheses of a variety of benzo[c]chromen-6-one derivatives were accomplished using Cs2CO3-promoted reactions between substituted 2-hydroxychalcones and β-ketoesters. These reactions involved domino Michael addition/intramolecular aldol/oxidative aromatization/lactonization and provided a rapid synthetic route for the production of biologically interesting novel benzo[c]chromen-6-one molecules bearing several different substituents on benzene rings. As an application of this methodology, several synthesized benzo[c]chromen-6-ones were transformed into highly functionalized novel terphenyls.

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Year:  2014        PMID: 24357122     DOI: 10.1039/c3ob41800f

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


  2 in total

1.  A metal-free aromative cascade for the synthesis of diverse heterocycles.

Authors:  Steven C Schlitzer; Dhanarajan Arunprasath; Katelyn G Stevens; Indrajeet Sharma
Journal:  Org Chem Front       Date:  2020-01-02       Impact factor: 5.281

2.  Oxidant-free, three-component synthesis of 7-amino-6H-benzo[c]chromen-6-ones under green conditions.

Authors:  B S Vachan; Aishwarya Ramesh; Muthu Karuppasamy; Isravel Muthukrishnan; Subbiah Nagarajan; J Carlos Menéndez; C Uma Maheswari; Vellaisamy Sridharan
Journal:  RSC Adv       Date:  2019-10-16       Impact factor: 4.036

  2 in total

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