Ruthenium-Catalyzed Straightforward Synthesis of 1,2,3,4-Tetrahydronaphthyridines via Selective Transfer Hydrogenation of Pyridyl Ring with Alcohols-Reference-Cited by-同舟云学术

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Ruthenium-Catalyzed Straightforward Synthesis of 1,2,3,4-Tetrahydronaphthyridines via Selective Transfer Hydrogenation of Pyridyl Ring with Alcohols

Published:2015-08-07 Issue:16 Volume:17 Page:4054-4057
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xiong Biao¹,Li Ya¹,Lv Wan¹,Tan Zhenda¹,Jiang Huanfeng¹,Zhang Min¹

Affiliation:

1. School of Chemistry & Chemical Engineering, South China University of Technology, Wushan Rd-381, Guangzhou 510641, People’s Republic of China

Funder

National Natural Science Foundation of China

Science Foundation for Distinguished Young Scholars of Guangdong Province

Ministry of Education of the People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b01976

Reference60 articles.

1. 117. Reduction by dissolving metals. Part I

2. A Mechanistic Analysis of the Birch Reduction

3. The True Identity of the Solvated Free Radical “Triphenylsilicyl Ethylammine.” The Multiple Addition of Lithium to an Aromatic System in Ethylamine

4. Reduction of Organic Compounds by Lithium in Low Molecular Weight Amines. I. Selective Reduction of Aromatic Hydrocarbons to Monoölefins

5. Catalytic hydrodeoxygenation of guaiacol over platinum supported on metal oxides and zeolites

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