Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Alina Eggert
  • Christoph Etling
  • Lucas Millbrodt
  • Göran Schulz
  • Markus Kalesse

Externe Organisationen

  • Helmholtz-Zentrum für Infektionsforschung GmbH (HZI)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)8722-8726
Seitenumfang5
FachzeitschriftOrganic letters
Jahrgang23
Ausgabenummer22
Frühes Online-Datum5 Nov. 2021
PublikationsstatusVeröffentlicht - 19 Nov. 2021

Abstract

A bisvinylogous Mukaiyama aldol reaction using oxazaborolidinones as a source of chirality was developed. This methodology allows the fast assembly of conjugated dienols by expanding the vinylogy principle by two additional carbons, and can be conducted using a readily available Lewis acid at reasonable reaction times. A broad range of aromatic and aliphatic aldehydes can be used providing access to complex building blocks for polyketide synthesis.

ASJC Scopus Sachgebiete

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Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction. / Eggert, Alina; Etling, Christoph; Millbrodt, Lucas et al.
in: Organic letters, Jahrgang 23, Nr. 22, 19.11.2021, S. 8722-8726.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Eggert A, Etling C, Millbrodt L, Schulz G, Kalesse M. Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction. Organic letters. 2021 Nov 19;23(22):8722-8726. Epub 2021 Nov 5. doi: 10.1021/acs.orglett.1c03165
Eggert, Alina ; Etling, Christoph ; Millbrodt, Lucas et al. / Oxazaborolidinone-Mediated Asymmetric Bisvinylogous Mukaiyama Aldol Reaction. in: Organic letters. 2021 ; Jahrgang 23, Nr. 22. S. 8722-8726.
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AU - Kalesse, Markus

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