Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/108109
Title: First Enantioselective Synthesis of Tetracyclic Intermediates en route to Madangamine D
Author: Amat Tusón, Mercedes
Ballette, Roberto
Proto, Stefano
Pérez Bosch, Maria
Bosch Cartes, Joan
Keywords: Alcaloides
Compostos heterocíclics
Estructura molecular
Alkaloids
Heterocyclic compounds
Molecular structure
Issue Date: 11-Mar-2013
Publisher: Royal Society of Chemistry
Abstract: The enantioselective synthesis of advanced tetracyclic precursors of madangamine D, bearing rings ABCD of this alkaloid, is reported. The saturated 14-membered ring is assembled from functionalized diazatricyclic intermediates 10 following either ring-closing metathesis or macrolactamization strategies.
Note: Versió postprint del document publicat a: https://doi.org/10.1039/C3CC41104D
It is part of: Chemical Communications, 2013, vol. 49, num. 30, p. 3149-3151
Related resource: https://doi.org/10.1039/C3CC41104D
URI: http://hdl.handle.net/2445/108109
ISSN: 1359-7345
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)

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