Intramolecular Pd-Mediated Processes of Amino-Tethered Aryl Halides and Ketones: Insight into the Ketone α-Arylation and Carbonyl-Addition Dichotomy. A New Class of Four-Membered Azapalladacycles-Reference-Cited by-同舟云学术

Intramolecular Pd-Mediated Processes of Amino-Tethered Aryl Halides and Ketones: Insight into the Ketone α-Arylation and Carbonyl-Addition Dichotomy. A New Class of Four-Membered Azapalladacycles

Published:2003-01-18 Issue:6 Volume:125 Page:1587-1594
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Solé Daniel¹,Vallverdú Lluís¹,Solans Xavier¹,Font-Bardía Mercè¹,Bonjoch Josep¹

Affiliation:

1. Contribution from the Laboratori de Química Orgànica, Facultat de Farmàcia, Universitat de Barcelona, Av. Joan XXIII s/n, 08028-Barcelona, and Departament de Cristal.lografia, Mineralogia i Dipòsits Minerals, Universitat de Barcelona, Martí i Franquès s/n, 08028-Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja029114w

Reference35 articles.

1. Palladium-Catalyzed Intramolecular Coupling of Vinyl Halides and Ketone Enolates. Synthesis of Bridged Azabicyclic Compounds

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