Literature DB >> 19545145

Biomimetic synthesis of a new class of bacterial signaling molecules.

Jesse B Davis1, J Daniel Bailey, Jason K Sello.   

Abstract

The first synthesis of a newly discovered class of bacterial signaling molecules from Streptomyces coelicolor has been developed. These molecules, known as the methylenomycin furans (MMFs), trigger production of the antibiotic methylenomycin. The synthesis features a scandium triflate-catalyzed domino reaction of beta-ketoesters and dihydroxyacetone yielding 2,3,4-substituted furans. The proposed reaction sequence (aldol reaction, cyclization, and dehydrative aromatization) may be reminiscent of the biosynthetic reaction in which dihydroxyacetone phosphate and a beta-ketothioester are condensed by an enzyme.

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Year:  2009        PMID: 19545145     DOI: 10.1021/ol9009893

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


  3 in total

1.  Preparation of 1,5-Dioxaspiro[5.5]undecan-3-one.

Authors:  Robert A Craig; Russell C Smith; Beau P Pritchett; Benzi I Estipona; Brian M Stoltz
Journal:  Organic Synth       Date:  2016

2.  Chemoenzymatic asymmetric synthesis of pregabalin precursors via asymmetric bioreduction of β-cyanoacrylate esters using ene-reductases.

Authors:  Christoph K Winkler; Dorina Clay; Simon Davies; Pat O'Neill; Paul McDaid; Sebastien Debarge; Jeremy Steflik; Mike Karmilowicz; John W Wong; Kurt Faber
Journal:  J Org Chem       Date:  2013-01-28       Impact factor: 4.354

3.  Signalling and Bioactive Metabolites from Streptomyces sp. RK44.

Authors:  Qing Fang; Fleurdeliz Maglangit; Linrui Wu; Rainer Ebel; Kwaku Kyeremeh; Jeanette H Andersen; Frederick Annang; Guiomar Pérez-Moreno; Fernando Reyes; Hai Deng
Journal:  Molecules       Date:  2020-01-22       Impact factor: 4.411

  3 in total

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