Magnetically Separable Pd Catalyst for Carbonylative Sonogashira Coupling Reactions for the Synthesis of α,β-Alkynyl Ketones-Reference-Cited by-同舟云学术

Magnetically Separable Pd Catalyst for Carbonylative Sonogashira Coupling Reactions for the Synthesis of α,β-Alkynyl Ketones

Published:2008-08-23 Issue:18 Volume:10 Page:3933-3936
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Jianming¹,Peng Xingao¹,Sun Wei¹,Zhao Yongwei¹,Xia Chungu¹

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, P. R. China, and Graduate School of the Chinese Academy of Sciences, Beijing, 100039, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol801478y

Reference47 articles.

1. A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO

2. Enantioselective Palladium-Catalyzed Transformations

3. Recent Advances in the Synthesis of Carbonyl Compounds by Palladium- Catalyzed Oxidative Carbonylation Reactions of Unsaturated Substrates

4. Evolution of Carbonylation Catalysis: No Need for Carbon Monoxide

5. Studies on copper(I) catalysed cross-coupling reactions : A convenient and facile method for the synthesis of diversely substituted α,β-acetylenic ketones

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