Advances in the vinylogous Mukaiyama aldol reaction and its application to the synthesis of the C1-C7 subunit of oleandolide

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OriginalspracheEnglisch
Seiten (von - bis)5093-5095
Seitenumfang3
FachzeitschriftTetrahedron letters
Jahrgang43
Ausgabenummer29
PublikationsstatusVeröffentlicht - 15 Juli 2002

Abstract

The synthesis of a stereo pentade of the macrolide antibiotic oleandolide is reported. The C1-C7 fragment resembles the analogous segment of Panek's total synthesis of oleandolide. The use of the vinylogous Mukaiyama aldol reaction shortens the route significantly and has the advantage of utilizing an easily accessible ketene acetal.

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Advances in the vinylogous Mukaiyama aldol reaction and its application to the synthesis of the C1-C7 subunit of oleandolide. / Hassfeld, Jorma; Kalesse, Markus.
in: Tetrahedron letters, Jahrgang 43, Nr. 29, 15.07.2002, S. 5093-5095.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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