Enantioselective Synthesis of Sterically Hindered Tertiary α-Aryl Oxindoles via Palladium-Catalyzed Decarboxylative Protonation. An Experimental and Theoretical Mechanistic Investigation-Reference-Cited by-同舟云学术

Enantioselective Synthesis of Sterically Hindered Tertiary α-Aryl Oxindoles via Palladium-Catalyzed Decarboxylative Protonation. An Experimental and Theoretical Mechanistic Investigation

Published:2018-07-19 Issue:16 Volume:360 Page:3124-3137
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Biosca Maria¹,Jackson Mark²,Magre Marc¹,Pàmies Oscar¹,Norrby Per-Ola³,Diéguez Montserrat¹,Guiry Patrick J.²

Affiliation:

1. Universitat Rovira i Virgili; Departament de Química Física i Inorgànica; C/Marcel.lí Domingo, 1 43007 Tarragona Spain

2. Centre for Synthesis and Chemical Biology, School of Chemistry; University College Dublin; Belfield, Dublin 4 Ireland

3. Early Product Development; Pharmaceutical Sciences, IMED Biotech Unit, AstraZeneca, Pepparedsleden 1; SE-431 83 Mölndal Sweden

Funder

Spanish Ministry of Economy and Competitiveness

European Regional Development Fund

Catalan Government

ICREA Foundation

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/adsc.201800507/fullpdf

Reference104 articles.

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4. Metallkatalysierte α-Arylierungen von Carbonylen und verwandten Molekülen: aktuelle Trends bei der C-C-Kupplung über C-H-Funktionalisierung

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