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Relevant bibliographies by topics / N-(Aryl)picolinamides

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Academic literature on the topic 'N-(Aryl)picolinamides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "N-(Aryl)picolinamides"

1

Xiao, Zhen, Juanjuan Li, Qiang Yue, Qian Zhang, and Dong Li. "An efficient and atom-economical route to N-aryl amino alcohols from primary amines." RSC Advances 8, no. 60 (2018): 34304–8. http://dx.doi.org/10.1039/c8ra07355d.

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2

Dasgupta, Moutusi, Haregewine Tadesse, Alexander J. Blake, and Samaresh Bhattacharya. "Interaction of N-(aryl)picolinamides with iridium. N–H and C–H bond activations." Journal of Organometallic Chemistry 693, no. 20 (2008): 3281–88. http://dx.doi.org/10.1016/j.jorganchem.2008.07.027.

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3

Xiao, Zhen, Sihao Shu, Yi Lin, Qian Zhang, Peng Ren, and Dong Li. "Chelation-Assisted C−N Cross-Coupling between Picolinamides and Aryl Boronic Acids under Nickel Catalysis." Asian Journal of Organic Chemistry 7, no. 10 (2018): 2053–56. http://dx.doi.org/10.1002/ajoc.201800441.

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4

Sankar, Rathinam, and Srinivasarao Arulananda Babu. "Construction of Tertiary Amides: NiII -Catalyzed N -Arylation of Secondary Acyclic Amides (2-Picolinamides) with Aryl Halides." Asian Journal of Organic Chemistry 6, no. 3 (2017): 269–73. http://dx.doi.org/10.1002/ajoc.201600596.

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5

Ipsita, Bhattacharya, Dasgupta Moutusi, G. B. Drew Michael, and Bhattacharya Samaresh. "N-(Aryl)picolinamide complexes of rhodium · Synthesis, structure and, spectral and electrochemical properties." Journal of Indian Chemical Society Vol. 89, Feb 2012 (2012): 205–16. https://doi.org/10.5281/zenodo.5758809.

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Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata-700 032, India <em>E-mail </em>: samaresh _ b@hotmail. com Department of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, UK <em>Manuscript received 20 December 2011, revised 30 December 2011, accepted 30 December 2011</em> Reaction of a series of <em>N</em>-(aryl)picolinamide ligands (HL-R, where H denotes the acidic proton and R<strong> </strong>(R=OCH<sub>3</sub><strong>, </strong>CH<sub>3</sub>,<strong> </strong>H, Cl and N0<sub>2</sub>) is the para substituent in the aryl fragment) with RhCI

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