Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/127700
Title: Pd0-Catalyzed Intramoleculara-Arylation of Sulfones: Domino Reactions in the Synthesis of Functionalized Tetrahydroisoquinolines
Author: Solé Arjó, Daniel
Pérez Janer, Ferran
Mancuso, Raffaella
Keywords: Compostos heterocíclics
Compostos de nitrogen
Compostos de sofre
Pal·ladi (Element químic)
Síntesi orgànica
Heterocyclic compounds
Nitrogen compounds
Sulfur compounds
Palladium
Organic synthesis
Issue Date: 10-Feb-2015
Publisher: Wiley-VCH
Abstract: A new strategy for the synthesis of tetrahydroisoquinolines based on the Pd(0)-catalyzed intramolecular α-arylation of sulfones is reported. The combination of this Pd-catalyzed reaction with intermolecular Michael and aza-Michael reactions allows the development of two- and three-step domino processes to synthesize diversely functionalized scaffolds from readily available starting materials. KEYWORDS: arylation; domino reactions; nitrogen heterocycles; palladium; sulfones
Note: Versió postprint del document publicat a: https://doi.org/10.1002/chem.201406305
It is part of: Chemistry-A European Journal, 2015, vol. 21, num. 12, p. 4580-4584
URI: http://hdl.handle.net/2445/127700
Related resource: https://doi.org/10.1002/chem.201406305
ISSN: 0947-6539
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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