169214-12-4Relevant articles and documents
Origin of the large isotope-induced shift in the 1H-NMR of ortho-2H-labelled anilides
Jones, John R.,Lockley, William J. S.,Lewis, Richard J.,Wilkinson, David J.
, p. 535 - 536 (2007)
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Digitally enhanced thin layer chromatography: Further development and some applications in isotopic chemistry
Manthorpe, Daniel P.,Lockley, William J. S.
, p. 544 - 552 (2013)
Improvements to thin layer chromatography (TLC) analysis can be made easily and cheaply by the application of digital colour photography and image analysis. The combined technique, digitally enhanced TLC (DE-TLC), is applicable to the accurate quantificat
Palladium-catalyzed trifluoromethylation of aromatic C-H bond directed by an acetamino group
Zhang, Li-Sheng,Chen, Kang,Chen, Guihua,Li, Bi-Jie,Luo, Shuang,Guo, Qing-Yun,Wei, Jiang-Bo,Shi, Zhang-Jie
supporting information, p. 10 - 13 (2013/04/10)
The first palladium-catalyzed ortho-trifluoromethylation of the aromatic C-H bond directed by an acetamino group is reported. This method provides an efficient and green approach to synthesize the highly biological potential key structure of ortho-CF3 acetanilides and anilines.
Highly effective Pd-catalyzed ortho olefination of acetanilides: Broad substrate scope and high tolerability
Kim, Byung Seok,Jang, Chungsik,Lee, Dong Jin,Youn, So Won
supporting information; experimental part, p. 2336 - 2340 (2011/06/25)
Bring it on! An effective Pd-catalyzed ortho olefination of various acetanilides has been developed. This transformation has a broad substrate scope and wide functional-group tolerability, regardless of the electronic and steric properties of acetanilide substrates, providing a straightforward access to highly functionalized arenes.
