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

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Original languageEnglish
Pages (from-to)5093-5095
Number of pages3
JournalTetrahedron letters
Volume43
Issue number29
Publication statusPublished - 15 Jul 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, Vol. 43, No. 29, 15.07.2002, p. 5093-5095.

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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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AU - Kalesse, Markus

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