1.
5-Mercaptotetrazoles as Synthetic Equivalents of Nitrogen-Contaning Functional Groups. The Case of the Organocatalytic Enantioselective aza-Michael Reaction
Uxue Uria, Efra m Reyes, Jose L. Vicario, Dolores Bad a, and Luisa Carrillo
Org. Lett., 2011, 13 (2), pp 336–339
Код: Выделить всё
http://dx.doi.org/10.1021/ol102892fThe Tetrazole 3-N-Oxide Synthesis
Tal Harel and Shlomo Rozen
J. Org. Chem., 2010, 75 (9), pp 3141–3143
Код: Выделить всё
http://dx.doi.org/10.1021/jo100278z3.
Synthesis and antiproliferative evaluation of 5-oxo and 5-thio derivatives of 1,4-diaryl tetrazoles Aditya S. Gundugola, Kusum Lata Chandra, Elisabeth M. Perchellet, Andrew M. Waters, Jean-Pierre H. Perchellet, Sundeep Rayat
Bioorganic & Medicinal Chemistry Letters, Volume 20, Issue 13, 1 July 2010, Pages 3920-3924
Код: Выделить всё
http://dx.doi.org/10.1016/j.bmcl.2010.05.0124.
Convenient Room-Temperature, Mercury-Assisted Synthesis of Tetrazoles by 1,3-Dipolar Cycloaddition†
Thomas M. Klapötke, Burkhard Krumm, Richard Moll
European Journal of Inorganic Chemistry
Volume 2011, Issue 3, pages 422–428, January 2011
Код: Выделить всё
http://dx.doi.org/10.1002/ejic.201001046Quantitative Structure–Electrochemistry Relationship of 1-Phenyl-5-benzyl-sulfanyltetrazoles and Their Electrooxidation as a Metabolic Model
Karel Nesměrák, Rafael Doležal, Věra Hudská, Josef Bártl, Martin Štícha, Karel Waisser
Electroanalysis
Volume 22, Issue 17-18, pages 2117–2122, September 2010
Код: Выделить всё
http://dx.doi.org/10.1002/elan.201000092