Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions

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OriginalspracheEnglisch
Seiten (von - bis)3561-3564
Seitenumfang4
FachzeitschriftOrganic letters
Jahrgang3
Ausgabenummer22
PublikationsstatusVeröffentlicht - 1 Nov. 2001

Abstract

(matrix presented) The use of the Z-configured vinylogous silyl ketene acetals in Mukaiyama aldol reactions is described, Isopropyl alcohol as scavanger and the use of tris(pentafluorophenyl)borane as the Lewis acid are required for obtaining the γ-alkylated syn-product selectively. In cases of α-chiral aldehydes, Felkin-Anh selectivity was observed.

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Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions. / Hassfeld, Jorma; Christmann, Mathias; Kalesse, Markus.
in: Organic letters, Jahrgang 3, Nr. 22, 01.11.2001, S. 3561-3564.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Hassfeld J, Christmann M, Kalesse M. Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions. Organic letters. 2001 Nov 1;3(22):3561-3564. doi: 10.1021/ol016677o
Hassfeld, Jorma ; Christmann, Mathias ; Kalesse, Markus. / Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions. in: Organic letters. 2001 ; Jahrgang 3, Nr. 22. S. 3561-3564.
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