Total synthesis of the antibiotic Elansolid B1

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OriginalspracheEnglisch
Seiten (von - bis)568-571
Seitenumfang4
FachzeitschriftOrganic Letters
Jahrgang16
Ausgabenummer2
PublikationsstatusVeröffentlicht - 17 Jan. 2014

Abstract

The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels-Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonogashira cross-coupling and a substratecontrolled Yamamoto aldol reaction.

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Total synthesis of the antibiotic Elansolid B1. / Weber, Arne; Dehn, Richard; Schläger, Nadin et al.
in: Organic Letters, Jahrgang 16, Nr. 2, 17.01.2014, S. 568-571.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Weber, A, Dehn, R, Schläger, N, Dieter, B & Kirschning, A 2014, 'Total synthesis of the antibiotic Elansolid B1', Organic Letters, Jg. 16, Nr. 2, S. 568-571. https://doi.org/10.1021/ol403441c
Weber, A., Dehn, R., Schläger, N., Dieter, B., & Kirschning, A. (2014). Total synthesis of the antibiotic Elansolid B1. Organic Letters, 16(2), 568-571. https://doi.org/10.1021/ol403441c
Weber A, Dehn R, Schläger N, Dieter B, Kirschning A. Total synthesis of the antibiotic Elansolid B1. Organic Letters. 2014 Jan 17;16(2):568-571. doi: 10.1021/ol403441c
Weber, Arne ; Dehn, Richard ; Schläger, Nadin et al. / Total synthesis of the antibiotic Elansolid B1. in: Organic Letters. 2014 ; Jahrgang 16, Nr. 2. S. 568-571.
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