Abstract:
A novel tellurium-containing heterocycle, 2H-1,4-benzotellurazin-3(4H)-one 1 has been prepared by treatment of butyl 2-aminophenyl telluride 2 with either bromoacetic acid or bromoacetyl chloride and subsequent elimination of butyl bromide from the tellurazinium compound 3 so formed.
Document Type:
Article
Language: English
Citation:
I. D. Sadekov, A. A. Maksimenko, G. M. Abakarov, Sh. S. Gasanov, V. A. Pantin, V. I. Minkin, “2H-1,4-Benzotellurazin-3(4H)-one and its Derivatives”, Mendeleev Commun., 3:2 (1993), 53–54
Linking options:
https://www.mathnet.ru/eng/mendc5262
https://www.mathnet.ru/eng/mendc/v3/i2/p53
This publication is cited in the following 6 articles:
Gabrielle Sanford, Kaitlynn E. Walker, Frank R. Fronczek, Thomas Junk, “Novel Organotellurium Heterocycles Derived From Bis(2‐Aminophenyl) Ditelluride”, Journal of Heterocyclic Chem, 54:1 (2017), 575
Jia‐fei Poon, Jiajie Yan, Vijay P. Singh, Paul J. Gates, Lars Engman, “Alkyltelluro Substitution Improves the Radical‐Trapping Capacity of Aromatic Amines”, Chemistry A European J, 22:36 (2016), 12891
Joshua P. Myers, Frank R. Fronczek, Thomas Junk, “The first crystal structures of six- and seven-membered tellurium- and nitrogen-containing (Te—N) heterocycles: 2H-1,4-benzotellurazin-3(4H)-one and 2,3-dihydro-1,5-benzotellurazepin-4(5H)-one”, Acta Crystallogr C Struct Chem, 72:1 (2016), 1
Nathan C. McMullen, Frank R. Fronczek, Thomas Junk, “Organotellurium Chemistry: Remarkably Facile Preparation of Benzo‐1,3‐tellurazoles”, Journal of Heterocyclic Chem, 50:1 (2013), 120
Igor D. Sadekov, Vladimir I. Minkin, Advances in Heterocyclic Chemistry, 79, 2001, 1
I. D. SADEKOV, A. A. MAKSIMENKO, G. M. ABAKAROV, S. S. GASANOV, V. A. PANTIN, V. I. MINKIN, “ChemInform Abstract: 2H‐1,4‐Benzotellurazin‐3(4H)‐one and Its Derivatives.”, ChemInform, 25:33 (1994)
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