Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: a new route to halogenated aromatic nitriles
…, S Pimparkar, M Jeganmohan
Index: Chinnagolla, Ravi Kiran; Pimparkar, Sandeep; Jeganmohan, Masilamani Chemical Communications, 2013 , vol. 49, # 30 p. 3146 - 3148
Full Text: HTML
Citation Number: 16
Abstract
The intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.
Related Articles:
Total synthesis of acerogenins E, G and K, and centrolobol
[Ogura, Tetsuhiro; Usuki, Toyonobu Tetrahedron, 2013 , vol. 69, # 13 p. 2807 - 2815]
[Wang, Azhong; Jiang, Huanfeng Journal of the American Chemical Society, 2008 , vol. 130, # 15 p. 5030 - 5031]
[Kaganovsky, Luba; Gelman, Dmitri; Rueck-Braun, Karola Journal of Organometallic Chemistry, 2010 , vol. 695, # 2 p. 260 - 266]
[Ushijima, Sousuke; Moriyama, Katsuhiko; Togo, Hideo Tetrahedron, 2012 , vol. 68, # 24 p. 4701 - 4709]
[Li, Pan; Zhao, Jingjing; Lang, Rui; Xia, Chungu; Li, Fuwei Tetrahedron Letters, 2014 , vol. 55, # 2 p. 390 - 393]