Palladium-Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3-Disubstituted 2,3-Dihydrobenzofuran-Reference-Cited by-同舟云学术

Palladium-Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3-Disubstituted 2,3-Dihydrobenzofuran

Published:2018-07-15 Issue:32 Volume:57 Page:10373-10377
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Zhang Zhan-Ming¹,Xu Bing¹,Qian Yanyan²,Wu Lizuo²,Wu Yuanqi²,Zhou Lujia¹,Liu Yu²,Zhang Junliang¹³^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical, Processes; School of Chemistry and Molecular Engineering; East China Normal University; Shanghai 200062 China

2. College of Chemistry and Life Science; Advanced Institute of Materials Science; Changchun University of Technology; Changchun 130012 China

3. Department of Chemistry; Fudan University; Shanghai 200438 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201806372/fullpdf

Reference84 articles.

1. Palladium-catalyzed conjugate addition reaction of aryl iodides with .alpha.,.beta.-unsaturated ketones

2. Conjugate addition vs. vinylic substitution in palladium-catalysed reaction of aryl halides with β-substituted-α,β-enones and -enals

3. The palladium-catalyzed hydroarylation and hydrovinylation of carbon-carbon multiple bonds: New perspectives in organic synthesis

4. The palladium-catalysed vinylic substitution of vinyl triflates with β-substituted-α,β-unsaturated carbonyl compounds. An application to the synthesis of cardenolides

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