Synthesis of 2-trifluoromethylquinolines through rhodium-catalysed redox-neutral [3 + 3] annulation between anilines and CF3-ynones using traceless directing groups
Literature Information
Haichao Huang, Hailong Wang, Chao Gong, Zhenjing Zhuang, Wenmin Feng, Si-Hai Wu, Lianhui Wang
Rhodium-catalysed regioselective redox-neutral [3 + 3]-cycloaddition of anilines with CF3-ynones was achieved via a traceless directing group strategy. A variety of substituted 2-trifluromethylquinoline compounds were obtained in good to excellent yields, which exhibited favorable blue emission properties.
Related Literature
Remote substituent effects on the photooxygenation of 9,10-diarylanthracenes: strong evidence for polar intermediates
Werner Fudickar, Torsten Linker
DOI: 10.1039/B719637G
Single molecule conformational analysis of the biologically relevant DNA G-quadruplex in the promoter of the proto-oncogene c-MYC
Pravin S. Shirude, Liming Ying, Shankar Balasubramanian
DOI: 10.1039/B801465E
Chemoenzymatic synthesis of prodigiosin analogues—exploring the substrate specificity of PigC
Suresh R. Chawrai, Neil R. Williamson, George P. C. Salmond, Finian J. Leeper
DOI: 10.1039/B719353J
An unusual dianion equivalent from acylsilanes for the synthesis of substituted β-keto esters
Chris V. Galliford, Karl A. Scheidt
DOI: 10.1039/B801597J
Photoinduced CO release, cellular uptake and cytotoxicity of a tris(pyrazolyl)methane (tpm) manganese tricarbonyl complex
Johanna Niesel, Antonio Pinto, Harmel W. Peindy N'Dongo, Klaus Merz, Ingo Ott, Ronald Gust, Ulrich Schatzschneider
DOI: 10.1039/B719075A
Isolation and X-ray structural characterization of tetraisopropylpyrene cation radical
Moloy Banerjee, Vijay S. Vyas, Sergey V. Lindeman, Rajendra Rathore
DOI: 10.1039/B800168E
Improved 3D DOSY-TOCSY experiment for mixture analysis
Stéphane Viel, Stefano Caldarelli
DOI: 10.1039/B802789G
Solid-state NMR studies of weak interactions in supramolecular systems
Michele R. Chierotti, Roberto Gobetto
DOI: 10.1039/B711551B
Size matters—strong binding of the terephthalate dianion by thiourea functionalised fused [n]polynorbornane hosts
Adam J. Lowe, Frederick M. Pfeffer
DOI: 10.1039/B801798K
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry












![1-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-benzo[d]imidazol-2(3H)-one structure 1-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-benzo[d]imidazol-2(3H)-one structure](https://static.chemtradehub.com/structs/603/60373-71-9-7dfb.webp)

