Dehydrogenative Syntheses of Biazoles via a “Pre-Join” Approach-Reference-Cited by-同舟云学术

Dehydrogenative Syntheses of Biazoles via a “Pre-Join” Approach

Published:2023-01-11 Issue:1 Volume:3 Page:80-85
ISSN:2691-3704
Container-title:JACS Au
language:en
Short-container-title:JACS Au

Author:

Yu Tianyang¹,Wang Yan¹,Dong Yaqun²,Han Derui¹,Liu Ning³^ORCID,Wang Bozhou³,Tang Yongxing²^ORCID,Wei Hao¹^ORCID

Affiliation:

1. Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi’an 710069, People’s Republic of China

2. School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, People’s Republic of China

3. Xi’an Modern Chemistry Research Institute, Xi’an 710065, People’s Republic of China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Key Research and Development Projects of Shaanxi Province

Publisher

American Chemical Society (ACS)

Subject

General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jacsau.2c00597

Reference56 articles.

1. Synthesis and antiprotozoal activity of methylnitro derivatives of 2,2'-biimidazole

2. Highly Efficient, Recyclable Pd(II) Catalysts with Bisimidazole Ligands for the Heck Reaction in Ionic Liquids

3. Recyclable Sonogashira coupling reactions in an ionic liquid, effected in the absence of both a copper salt and a phosphineElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b4/b402477j/

4. An Ionic Liquid-Coordinated Palladium Complex: A Highly Efficient and Recyclable Catalyst for the Heck Reaction

5. Synthesis of 2,2‘-Biimidazolium-Based Ionic Liquids: Use as a New Reaction Medium and Ligand for Palladium-Catalyzed Suzuki Cross-Coupling Reactions

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