Symmetrical Biaryls from Diazotized Amines. Reducing Agents. II

ER Atkinson, D Holm-Hansen, AD Nevers…

Index: Atkinson et al. Journal of the American Chemical Society, 1943 , vol. 65, p. 476

Full Text: HTML

Citation Number: 5

Abstract

We have continued our systematic examination'of those reducing agents which might convert diazotized amines to symmetrical biaryls. As in the previous work diazotized anthranilic acid has been used and the work has been confined to aqueous solutions. None of the agents here described are as effective as those previously studied but our results are of interest because the use of" standard" conditions and a single diazotized amine makes ...

Related Articles:

Synthesis of C8-linked pyrrolo [2, 1-c][1, 4] benzodiazepine-acridone/acridine hybrids as potential DNA-binding agents

[Kamal, Ahmed; Srinivas; Ramulu; Ramesh; Kumar, P. Praveen Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 15 p. 4107 - 4111]

Developing bivalent ligands to target CUG triplet repeats, the causative agent of myotonic dystrophy type 1

[Jahromi, Amin Haghighat; Fu, Yuan; Miller, Kali A.; Nguyen, Lien; Luu, Long M.; Baranger, Anne M.; Zimmerman, Steven C. Journal of Medicinal Chemistry, 2013 , vol. 56, # 23 p. 9471 - 9481]

Convenient access to substituted acridines by a Buchwald–Hartwig amination

[Csuk, Rene; Barthel, Alexander; Raschke, Christian Tetrahedron, 2004 , vol. 60, # 27 p. 5737 - 5750]

Convenient access to substituted acridines by a Buchwald–Hartwig amination

[Csuk, Rene; Barthel, Alexander; Raschke, Christian Tetrahedron, 2004 , vol. 60, # 27 p. 5737 - 5750]

Convenient access to substituted acridines by a Buchwald–Hartwig amination

[Csuk, Rene; Barthel, Alexander; Raschke, Christian Tetrahedron, 2004 , vol. 60, # 27 p. 5737 - 5750]

More Articles...