Synthesis of the northern hemisphere of epothilone A by a ten-membered ring closing metathesis reaction

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Original languageEnglish
Pages (from-to)3553-3556
Number of pages4
JournalTetrahedron letters
Volume40
Issue number18
Publication statusPublished - 30 Apr 1999

Abstract

The synthesis of the strained epothilone analog containing a ten- membered ring as well as the northern hemisphere of epothilone A is described. This approach, using the ring closing metathesis reaction, is a solution to the lack of stereocontrol observed in the ring closing metathesis reaction utilized in the synthesis of the epothilone backbone by other groups.

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Synthesis of the northern hemisphere of epothilone A by a ten-membered ring closing metathesis reaction. / Gerlach, Kai; Quitschalle, Monika; Kalesse, Markus.
In: Tetrahedron letters, Vol. 40, No. 18, 30.04.1999, p. 3553-3556.

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Gerlach K, Quitschalle M, Kalesse M. Synthesis of the northern hemisphere of epothilone A by a ten-membered ring closing metathesis reaction. Tetrahedron letters. 1999 Apr 30;40(18):3553-3556. doi: 10.1016/S0040-4039(99)00550-X
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AU - Kalesse, Markus

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