A novel Sm(II) - induced route to highly substituted benzannulated cyclooctanol derivatives

Khan, Faiz Ahmed ; Czerwonka, Regina ; Zimmer, Reinhold ; Reissig, Hans-Ulrich (1997) A novel Sm(II) - induced route to highly substituted benzannulated cyclooctanol derivatives Synlett, 1997 (8). pp. 995-997. ISSN 0936-5214

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Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-1997-934

Abstract

Siloxycyclopropane derivatives 3 with a suitable styrene side chain can effectively be ring opened to precursors 2 which undergo reductive ring closure with SmI2 to furnish benzannulated cyclooctanols 1 or lactones 7 derived thereof. Tricyclic lactone 7c can be further substituted by conversion into a bridgehead enolate and reactions with electrophiles.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Siloxycyclopropanes; Samarium(II) Iodide; Stille Coupling; Cyclooctanol; Alkylation
ID Code:80349
Deposited On:31 Jan 2012 14:25
Last Modified:31 Jan 2012 14:25

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