Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones-Reference-Cited by-同舟云学术

Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones

Published:2016-04-05 Issue:8 Volume:18 Page:1872-1875
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fu Wai Chung¹,So Chau Ming¹,Yuen On Ying¹,Lee Irene Toi Chuk¹,Kwong Fuk Yee¹

Affiliation:

1. State Key Laboratory of Chirosciences and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong

Funder

Research Grants Council, University Grants Committee, Hong Kong

State Key Laboratory of Chirosciences, Hong Kong Polytechnic University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b00643

Reference60 articles.

1. Palladium-Catalyzed α-Arylation Reactions in Total Synthesis

2. Metal-Catalyzed α-Arylation of Carbonyl and Related Molecules: Novel Trends in CC Bond Formation by CH Bond Functionalization

3. Palladium-Catalyzed α-Arylation of Carbonyl Compounds and Nitriles

4. Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides

5. Pd-catalyzed α-Arylation of Carbonyl and Related Compounds: Recent Developments and Perspectives

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