Ruthenium Catalyzed C–H Selenylations of Aryl Acetic Amides and Esters via Weak Coordination-Reference-Cited by-同舟云学术

Ruthenium Catalyzed C–H Selenylations of Aryl Acetic Amides and Esters via Weak Coordination

Published:2019-08-05 Issue:16 Volume:21 Page:6310-6314
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Weng Zhengyun¹,Fang Xinyue¹,He Meicui¹,Gu Linghui¹,Lin Jiafu¹,Li Zheyu¹,Ma Wenbo¹^ORCID

Affiliation:

1. Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province, Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu 610052, P.R. China

Funder

Department of Science and Technology of Sichuan Province

Youth foundation of Chengdu University

Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02196

Reference75 articles.

1. Synthesis and antiinflammatory activity of [(cycloalkylmethyl)phenyl]acetic acids and related compounds

2. Increased Hydrophobicity and Estrogenic Activity of Simple Phenols with Silicon and Germanium-Containing Substituents

3. Syntheses and Properties of Silicon- and Germanium-Containing α-Amino Acids and Peptides: A Study on C/Si/Ge Bioisosterism

4. Antiinflammatory agents. 4. Syntheses and biological evaluation of potential pro-drugs of 2-amino-3-benzoylbenzeneacetic acid and 2-amino-3-(4-chlorobenzoyl)benzeneacetic acid

5. Substituent effects upon the base hydrolysis of penicillins and cephalosporins. Competitive intramolecular nucleophilic amino attack in cephalosporins

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