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- Copper catalyzed cyanation through CC bond cleavage of gem-aryl dibromide followed by second cyanation of iodoarene by a released CN unit. Pintu Maity, Debasish Kundu, Tubai Ghosh, Brindaban C. Ranu
, Org. Chem. Front.
, 2018
, 5
, 1586
- NBS mediated nitriles synthesis through CC double bond cleavage. Xiaolin Zong, Qing-Zhong Zheng, Ning Jiao
, Org. Biomol. Chem.
, 2014
, 12
, 1198
- Lithium amide catalyzed hydroboration of nitriles. Pradip Ghosh, Axel Jacobi von Wangelin
, Org. Chem. Front.
, 2020
, 7
, 960
- The diverse photocycloaddition reactions of 4-methoxybenzonitrile: novel formation of azacyclo-octatetraenes. Nader Al-Jalal, Michael G. B. Drew, Andrew Gilbert
, J. Chem. Soc., Chem. Commun.
, 1985
, 85
- Sandmeyer reactions. Part 6.1 A mechanistic investigation into the reduction and ligand transfer steps of Sandmeyer cyanation. Peter Hanson, Simon C. Rowell, Alec B. Taylor, Paul H. Walton, Allan W. Timms
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 1126
- Clear piezochromic behaviors of AIE-active organic powders under hydrostatic pressure. Mi Ouyang, Lingling Zhan, Xiaojing Lv, Feng Cao, Weijun Li, Yujian Zhang, Kunyan Wang, Cheng Zhang
, RSC Adv.
, 2016
, 6
, 1188
- CuI-mediated synthesis of 1-aryl-5,6,7-trimethoxybenzimidazoles as potent antitubulin agents. Cong-Min Peng, Shih-Wei Wang, Yi-Lin Hwang, Wen-Chun Sun, Li-Pin Chiu, Yi-Ting Liu, Yu-Wei Lai, Hsueh-Yun Lee
, RSC Adv.
, 2023
, 13
, 13169
- Copper-free Sandmeyer cyanation of arenediazonium o-benzenedisulfonimides. Margherita Barbero, Silvano Cadamuro, Stefano Dughera
, Org. Biomol. Chem.
, 2016
, 14
, 1437
- A non-metal catalysed oxidation of primary azides to nitriles at ambient temperature. Manjunath Lamani, Pradeep Devadig, Kandikere Ramaiah Prabhu
, Org. Biomol. Chem.
, 2012
, 10
, 2753
- Ex situ generation of stoichiometric HCN and its application in the Pd-catalysed cyanation of aryl bromides: evidence for a transmetallation step between two oxidative addition Pd-complexes. Steffan K. Kristensen, Espen Z. Eikeland, Esben Taarning, Anders T. Lindhardt, Troels Skrydstrup
, Chem. Sci.
, 2017
, 8
, 8094