Stereoselective Palladium-Catalyzed α-Arylation of 3-Aryl-1-Indanones: An Asymmetric Synthesis of (+)-Pauciflorol F-Reference-Cited by-同舟云学术

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Stereoselective Palladium-Catalyzed α-Arylation of 3-Aryl-1-Indanones: An Asymmetric Synthesis of (+)-Pauciflorol F

Published:2011-07-22 Issue:16 Volume:76 Page:6611-6618
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lee Bong Hyang¹²,Choi Young Lok¹³,Shin Seunghoon²,Heo Jung-Nyoung¹

Affiliation:

1. Medicinal Chemistry Research Center, Korea Research Institute of Chemical Technology, 100 Jang-dong, Daejeon 305-600, Korea

2. Department of Chemistry, Hanyang University, 17 Haengdang-dong, Seoul 133-791, Korea

3. Department of Chemistry, Korea University, Anam-dong, Seoul 105-600 Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo2009164

Reference44 articles.

1. 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

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

3. Microwave-promoted synthesis of amino-substituted 2-pyridone derivatives via palladium-catalyzed amination reaction

4. An efficient procedure for the synthesis of 3-aryl-4-methoxy-2(5H)-furanones by using the microwave-promoted Suzuki–Miyaura coupling reactions

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