Insights into the Mechanism of Anodic N–N Bond Formation by Dehydrogenative Coupling-Reference-Cited by-同舟云学术

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Insights into the Mechanism of Anodic N–N Bond Formation by Dehydrogenative Coupling

Published:2017-08-28 Issue:35 Volume:139 Page:12317-12324
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gieshoff Tile¹²³,Kehl Anton¹,Schollmeyer Dieter¹,Moeller Kevin D.³^ORCID,Waldvogel Siegfried R.¹²^ORCID

Affiliation:

1. Institute of Organic Chemistry, Johannes Gutenberg University Mainz, 55128 Mainz, Germany

2. Graduate School Materials Science in Mainz, Johannes Gutenberg University Mainz, 55128 Mainz, Germany

3. Department of Chemistry, Washington University, St. Louis, Missouri 63130, United States

Funder

Carl-Zeiss-Stiftung

Deutsche Forschungsgemeinschaft

National Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b07488

Reference52 articles.

1. Prediction of genotoxic potential of cosmetic ingredients by an in silico battery system consisting of a combination of an expert rule-based system and a statistics-based system

2. Synthesis, in vitro and in vivo anticancer activities of novel 4-substituted 1,2-bis(4-chlorophenyl)-pyrazolidine-3,5-dione derivatives

3. JTP-426467 acts as a selective antagonist for peroxisome proliferator-activated receptor ? in vitro and in vivo

4. Pyrazolidine-3,5-dione derivatives as potent non-steroidal agonists of farnesoid X receptor: Virtual screening, synthesis, and biological evaluation

5. Pyrazolidine-3,5-diones and 5-Hydroxy-1H-pyrazol-3(2H)-ones, Inhibitors of UDP-N-acetylenolpyruvyl Glucosamine Reductase

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