Oxidative Addition of Aryl Chlorides to Monoligated Palladium(0): A DFT-SCRF Study-Reference-Cited by-同舟云学术

Oxidative Addition of Aryl Chlorides to Monoligated Palladium(0): A DFT-SCRF Study

Published:2007-01-01 Issue:3 Volume:26 Page:550-553
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Ahlquist Mårten¹,Norrby Per-Ola¹

Affiliation:

1. Departments of Chemistry, Technical University of Denmark, Building 201 Kemitorvet, DK-2800 Kgs. Lyngby, Denmark, and Göteborg University, Kemigården 4, SE-412 96 Göteborg, Sweden

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om0604932

Reference37 articles.

1. A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium

2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

3. Selective carbon-carbon bond formation via transition metal catalysts. 9. Double metal catalysis in the cross-coupling reaction and its application to the stereo- and regioselective synthesis of trisubstituted olefins

4. Arylation of Olefin with Aryl Iodide Catalyzed by Palladium

5. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides

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