Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/127810
Title: Exploring Partners for the Domino α‐Arylation/Michael Addition Reaction Leading to Tetrahydroisoquinolines
Author: Solé Arjó, Daniel
Pérez Janer, Ferran
García-Rodeja Navarro, Yago
Fernández Cadenas, Israel
Keywords: Pal·ladi (Element químic)
Catàlisi
Sulfamides
Teoria del funcional de densitat
Síntesi orgànica
Palladium
Catalysis
Sulfonamides
Density functionals
Organic synthesis
Issue Date: 3-Jan-2017
Publisher: Wiley-VCH
Abstract: Sulfonates, sulfonamides, and phosphonates have proven useful nucleophiles for palladium‐catalyzed intramolecular α‐arylation reactions leading to tetrahydroisoquinolines. Although the sulfonate α‐arylation reaction can be successfully combined in a domino process with a broad range of Michael acceptors, only vinyl sulfones can be used in Michael additions when starting from sulfonamides. No domino process was developed with the phosphonate derivative. DFT calculations were carried out to gain more insights into the experimental differences observed in the reactions involving these substrates.
Note: Versió postprint del document publicat a: https://doi.org/10.1002/ejoc.201601300
It is part of: European Journal of Organic Chemistry, 2017, vol. 2017, num. 4, p. 799-805
URI: http://hdl.handle.net/2445/127810
Related resource: https://doi.org/10.1002/ejoc.201601300
ISSN: 1434-193X
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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