Mechanism and Stereoselectivity of Directed C(sp3)–H Activation and Arylation Catalyzed by Pd(II) with Pyridine Ligand and Trifluoroacetate: A Computational Study-Reference-Cited by-同舟云学术

Mechanism and Stereoselectivity of Directed C(sp3)–H Activation and Arylation Catalyzed by Pd(II) with Pyridine Ligand and Trifluoroacetate: A Computational Study

Published:2015-05-18 Issue:6 Volume:5 Page:3648-3661
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Jiang Julong¹,Yu Jin-Quan²,Morokuma Keiji¹

Affiliation:

1. Fukui Institute for Fundamental Chemistry, Kyoto University, Kyoto 606-8103, Japan

2. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cs501626n

Reference71 articles.

1. Carbon−Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts

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

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

4. Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides

5. The Palladium-Catalyzed Cross-Coupling Reactions of Organotin Reagents with Organic Electrophiles[New Synthetic Methods(58)]

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