Perkin communications: Iodonium-induced cyclisations of 5-silylalk-4-enols

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  • Universität Hamburg
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OriginalspracheEnglisch
Seiten (von - bis)1481-1483
Seitenumfang3
FachzeitschriftJournal of the Chemical Society, Perkin Transactions 1
Ausgabenummer5
PublikationsstatusVeröffentlicht - 1990
Extern publiziertJa

Abstract

In the presence of hypervalent iodine reagents, silyl-substituted δ,ε-unsaturated alcohols (4a-f) underwent ring-closure to give the pyran-3-ones (5) as well as tosyloxy substituted tetrahydropyrans (6) and (7).

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Perkin communications: Iodonium-induced cyclisations of 5-silylalk-4-enols. / Schaumann, Ernst; Kirschning, Andreas.
in: Journal of the Chemical Society, Perkin Transactions 1, Nr. 5, 1990, S. 1481-1483.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Schaumann, E & Kirschning, A 1990, 'Perkin communications: Iodonium-induced cyclisations of 5-silylalk-4-enols', Journal of the Chemical Society, Perkin Transactions 1, Nr. 5, S. 1481-1483. https://doi.org/10.1039/P19900001481
Schaumann, E., & Kirschning, A. (1990). Perkin communications: Iodonium-induced cyclisations of 5-silylalk-4-enols. Journal of the Chemical Society, Perkin Transactions 1, (5), 1481-1483. https://doi.org/10.1039/P19900001481
Schaumann E, Kirschning A. Perkin communications: Iodonium-induced cyclisations of 5-silylalk-4-enols. Journal of the Chemical Society, Perkin Transactions 1. 1990;(5):1481-1483. doi: 10.1039/P19900001481
Schaumann, Ernst ; Kirschning, Andreas. / Perkin communications : Iodonium-induced cyclisations of 5-silylalk-4-enols. in: Journal of the Chemical Society, Perkin Transactions 1. 1990 ; Nr. 5. S. 1481-1483.
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