Abstract—(±)-Botryodiplodin and (±)-epi-botryodiplodin acetates were prepared in good yields following a practical four step route. The method, for the construction of the strategic tetrahydrofuran ring, hinged on an unprecedented halogen atom transfer Ueno–Stork cyclization of an O-allyl a,a-dihalohemiacetal acetate, catalyzed by the redox complex CuCl/N,N,N0,N00,N00-pentamethyldiethylenetriamine.
A new and effective route to (±)-botryodiplodin and (±)-epi-botryodiplodin acetates using a halogen atom transfer Ueno-Stork cyclization / L., DE BUYCK; Forzato, Cristina; F., Ghelfi; A., Mucci; Nitti, Patrizia; U. M., Pagnoni; A. F., Parsons; Pitacco, Giuliana; F., Roncaglia. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - STAMPA. - 47:(2006), pp. 7759-7762. [10.1016/j.tetlet.2006.08.121]
A new and effective route to (±)-botryodiplodin and (±)-epi-botryodiplodin acetates using a halogen atom transfer Ueno-Stork cyclization
FORZATO, Cristina;NITTI, PATRIZIA;PITACCO, GIULIANA;
2006-01-01
Abstract
Abstract—(±)-Botryodiplodin and (±)-epi-botryodiplodin acetates were prepared in good yields following a practical four step route. The method, for the construction of the strategic tetrahydrofuran ring, hinged on an unprecedented halogen atom transfer Ueno–Stork cyclization of an O-allyl a,a-dihalohemiacetal acetate, catalyzed by the redox complex CuCl/N,N,N0,N00,N00-pentamethyldiethylenetriamine.Pubblicazioni consigliate
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