Literature DB >> 25518892

A microwave-assisted multicomponent synthesis of substituted 3,4-dihydroquinazolinones.

Marc Y Stevens1, Krzysztof Wieckowski, Peng Wu, Rajiv T Sawant, Luke R Odell.   

Abstract

A microwave-assisted, multicomponent protocol for the synthesis of substituted 3,4-dihydroquinazolinones via a novel cascade imine/cyclization/aza-Henry reaction sequence is reported. Starting from o-formyl carbamates, a series of structurally diverse 3,4-dihydroquinazolinones was synthesized via a cyclic iminium ion intermediate in moderate to excellent yields. Notably, the reaction is fast, flexible, simple to perform and tolerates a variety of functional groups.

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Year:  2015        PMID: 25518892     DOI: 10.1039/c4ob02417f

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


  2 in total

1.  Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents.

Authors:  Fahimeh Taayoshi; Aida Iraji; Ali Moazzam; Meysam Soleimani; Mehdi Asadi; Keyvan Pedrood; Mosayeb Akbari; Hafezeh Salehabadi; Bagher Larijani; Neda Adibpour; Mohammad Mahdavi
Journal:  BMC Chem       Date:  2022-05-18

2.  Synthesis of substituted 3,4-dihydroquinazolinones via a metal free Leuckart-Wallach type reaction.

Authors:  Suvarna Bokale-Shivale; Mohammad A Amin; Rajiv T Sawant; Marc Y Stevens; Lewend Turanli; Adam Hallberg; Suresh B Waghmode; Luke R Odell
Journal:  RSC Adv       Date:  2020-12-23       Impact factor: 3.361

  2 in total

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