Results 151 to 160 of about 6,074 (218)

Hyperbranched Polysiloxane-Copper(II) Pyridylamine-Glycidoxypropyltrimethoxysilane Complex-Catalyzed Click Reactions under Mild Conditions. [PDF]

ACS Omega
Borzooei M, Norouzi M, Mohammadi M.
europepmc   +1 more source

Activation of TREK-1 and TREK-2 Two-Pore Domain Potassium Channels by the K_v4 Channel Modulator, NS5806. [PDF]

Pharmacol Res Perspect
Veale EL, Matthews PM, Rush AM, Stevens EB, Mathie A.   +4 more
europepmc   +1 more source

In situ synthesis of ultrafine Cu(ii) metal immobilized on pectin hydrogel, modified by a CoFe₂O₄/Pr-SO₃H nanocomposite as a green catalyst for reduction of nitro compounds and synthesis of 1H-tetrazoles. [PDF]

RSC Adv
Mozafari R, Mohammadi M, Moradi S, Ghadermazi M.   +3 more
europepmc   +1 more source

Periodic mesoporous organosilica functionalized with <i>p</i>-aminobenzenesulfonic acid: an efficient solid acid catalyst for one-pot synthesis of 5-substituted 1<i>H</i>-tetrazoles under eco-friendly conditions. [PDF]

Nanoscale Adv
Fanimoghadam H, Dekamin MG, Naimi-Jamal MR.   +2 more
europepmc   +1 more source

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The Chemistry of the Tetrazoles.

Chemical Reviews, 1947
exaly   +3 more sources

Nitroimino-tetrazolates and Oxy-nitroimino-tetrazolates

Journal of the American Chemical Society, 2010
Highly energetic 1,1'-ethylenebis(oxy)bis(5-nitroimino-tetrazolate) salts were obtained by reacting equimolar quantities of the acidic 1,1'-ethylenebis(oxy)bis(5-nitroimino-tetrazole) and energetic bases in aqueous solution. Additionally, metathesis of silver 1,1'-ethylenebis(oxy)bis(5-nitroimino-tetrazolate) with diaminoguanidinium chloride or ...
Young-Hyuk, Joo, Jean'ne M, Shreeve
openaire   +2 more sources

Iodine-Catalyzed, Efficient, One-Pot Protocol for the Conversion of Araldehydes Into 5-Aryl-1H-Tetrazoles

Synthetic Communications, 2011
An easy access to various 5-aryl-1H-tetrazoles by a one-pot direct conversion of aldehydes to tetrazoles without the isolation of the intermediate nitriles using commercially available iodine as a catalyst is described.
Mohamed Afzal Pasha, M B Madhusudana Reddy   +1 more
exaly   +2 more sources

Tetrazoles

2008
V.A. Ostrovskii, G.I. Koldobskii, R.E. Trifonov   +2 more
exaly   +2 more sources

Relation between the substituent effect and aromaticity in tetrazoles, protonated tetrazoles and tetrazolate derivatives

Journal of Molecular Structure: THEOCHEM, 2007
Abstract The energies, geometries and aromaticity of a series of 5R tetrazoles [R = NH 2 , OH, OCH 3 , SCH 3 , H, CH 3 , F, Cl, BH 2 , CF 3 , CN, NO, NO 2 ], their anions and protonated forms in the gas phase have been calculated with the DFT/B3LYP method at the 6-31++G ∗∗ level.
Alireza Najafi Chermahini, Hossein Abdol Dabbagh, Abbas Teimouri   +2 more
openaire   +1 more source