Thiol-free chemoenzymatic synthesis of β-ketosulfides

A preparation of β-ketosulfides avoiding the use of thiols is described. The combination of a multicomponent reaction and a lipase-catalysed hydrolysis has been developed in order to obtain high chemical diversity employing a single sulfur donor. This methodology for the selective synthesis of a set...

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Veröffentlicht in:Beilstein journal of organic chemistry 2019-02, Vol.15 (1), p.378-387
Hauptverfasser: Heredia, Adrián A, López-Vidal, Martín G, Kurina-Sanz, Marcela, Bisogno, Fabricio R, Peñéñory, Alicia B
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Sprache:eng
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Zusammenfassung:A preparation of β-ketosulfides avoiding the use of thiols is described. The combination of a multicomponent reaction and a lipase-catalysed hydrolysis has been developed in order to obtain high chemical diversity employing a single sulfur donor. This methodology for the selective synthesis of a set of β-ketosulfides is performed under mild conditions and can be set up in one-pot two-step and on a gram-scale.
ISSN:1860-5397
2195-951X
1860-5397
DOI:10.3762/bjoc.15.34