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Reactions of organotin tetrazoles: synthesis of functionalised poly-tetrazoles

Journal of the Chemical Society, Perkin Transactions 1, 1999
Reaction of 1,2-bis[2-(tributylstannyl)tetrazol-5-yl]benzene with 1,2-dibromoethane (1∶10) yields the 1-N,1-N′-ethylene bridged cyclophane (1) while similar reactions with larger excesses (1∶25) of 1,n-dibromoalkanes yield 1,2-bis[2-(bromoalkyl)tetrazol-5-yl]benzenes along with the unsymmetrical 1-N,2-N-substituted tetrazole isomers. Analogous products
Paul A. Bethel   +3 more
openaire   +1 more source

Tetrazoles for biomedicine

Russian Chemical Reviews, 2019
The tetrazole ring is an important pharmacophore. It is a structural component in many drugs, drug candidates (or lead compounds) and various biochemical reagents.
Elena A. Popova   +2 more
openaire   +1 more source

Tetrazoles: XLIX. Alkylation of tetrazoles with tetrakis(chloroacetoxymethyl)methane

Russian Journal of Organic Chemistry, 2006
Alkylation of 1-aryl-4,5-dihydro-1H-tetrazol-5-ones and 1-phenyl-4,5-dihydro-1H-tetrazole-5-thione with tetrakis(2-chloroacetoxymethyl)methane in boiling acetonitrile in the presence of potassium bromide and triethylamine gives tetrakis[2-(4-aryl-5-oxo-4,5-dihydro-1H-tetrazol-1-yl)acetoxymethyl]-methanes and tetrakis[2-(1-phenyl-1H-tetrazol-5 ...
M. V. Zatsepina   +2 more
openaire   +1 more source

The Hydrogen Bond Environments of 1H-Tetrazole and Tetrazolate Rings: The Structural Basis for Tetrazole–Carboxylic Acid Bioisosterism

Journal of Chemical Information and Modeling, 2012
Bioisosterism involving replacement of a carboxylic acid substituent by 1H-tetrazole, yielding deprotonated carboxylate and tetrazolate under physiological conditions, is a well-known synthetic strategy in medicinal chemistry. To improve our overall understanding of bioisosterism, we have used this example to study the geometrical and energetic aspects
Frank H. Allen   +5 more
openaire   +2 more sources

Theoretical study of synthetic reaction of tetrazole and tetrazolate anion

International Journal of Quantum Chemistry, 2000
Tetrazole (H2CN4) and tetrazolate anion (HCN) are high-energy compounds with a five-membered ring-type structures, which can be easily synthesized by HCN and HN3 and by HCN and N, respectively, in an irreversible reaction. The ab initio methods including MP2/6-31G**, B3LYP/6-31G**, B3LYP/6-311+G(2d,p), and CBS/QB3 from Gaussian 98 program are employed ...
openaire   +1 more source

Tetrazoles

Russian Chemical Reviews, 1994
Meier, Hans Rudolf, Heimgartner, Heinz
openaire   +2 more sources

Tetrazoles

2022
Vladimir A. Ostrovskii   +2 more
openaire   +1 more source

Tetrazole Derivatives. III. Tetrazole Acid Derivatives

The Journal of Organic Chemistry, 1956
R. A. LaFORGE   +3 more
openaire   +1 more source

Functionalized Tetrazole Energetics: A Route to Enhanced Performance

Zeitschrift Fur Anorganische Und Allgemeine Chemie, 2021
Jean'Ne M Shreeve   +2 more
exaly  

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