Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes

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OriginalspracheEnglisch
Seiten (von - bis)1263-1265
Seitenumfang3
FachzeitschriftTetrahedron letters
Jahrgang42
Ausgabenummer7
PublikationsstatusVeröffentlicht - 12 Feb. 2001

Abstract

Natural products like ratjadone and callystatin A contain an α,β-unsaturated lactone moiety which adds to the biological activity of these compounds. Here we report a rapid and practical access to lactone precursor 3 by an asymmetric hetero Diels-Alder reaction as the key step and its subsequent transformation into a suitable building block 4.

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Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes. / Quitschalle, Monika; Christmann, Mathias; Bhatt, Ulhas et al.
in: Tetrahedron letters, Jahrgang 42, Nr. 7, 12.02.2001, S. 1263-1265.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Quitschalle M, Christmann M, Bhatt U, Kalesse M. Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes. Tetrahedron letters. 2001 Feb 12;42(7):1263-1265. doi: 10.1016/S0040-4039(00)02213-9
Quitschalle, Monika ; Christmann, Mathias ; Bhatt, Ulhas et al. / Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes. in: Tetrahedron letters. 2001 ; Jahrgang 42, Nr. 7. S. 1263-1265.
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