Literature DB >> 15957931

Microwave-enhanced synthesis of N-shifted buflavine analogues via a Suzuki-ring-closing metathesis protocol.

Prasad Appukkuttan1, Wim Dehaen, Erik Van der Eycken.   

Abstract

[reaction: see text] A novel, microwave-enhanced six-step synthesis was devised for the synthesis of N-shifted buflavine analogues. Microwave-enhanced Suzuki-Miyaura cross-coupling and ring-closing metathesis reactions were used as the key steps. Microwave irradiation was found to enhance the ring-closing metathesis reaction to generate the otherwise difficultly obtainable medium-sized ring system of the target molecules.

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Year:  2005        PMID: 15957931     DOI: 10.1021/ol050806+

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

Review 2.  Microwave-Assisted Syntheses of Bioactive Seven-Membered, Macro-Sized Heterocycles and Their Fused Derivatives.

Authors:  Mohsine Driowya; Aziza Saber; Hamid Marzag; Luc Demange; Khalid Bougrin; Rachid Benhida
Journal:  Molecules       Date:  2016-08-09       Impact factor: 4.411

  2 in total

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