Skip to search formSkip to main contentSkip to account menu

Tetrazoles

Known as: Tetrazoles [Chemical/Ingredient] 
National Institutes of Health

Related topics

Related topics

50 relations

Narrower (46)

1,3,5-benzenetristetrazolate1-(tetrazol-5-yl)ethanol1-N-methyl-5-thiotetrazole1-phenyl-5-mercaptotetrazole
In Bloodagonistsantagonists & inhibitorschemical synthesis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Photo-induced coupling reactions of tetrazoles with carboxylic acids in aqueous solution: application in protein labelling.
The photo-induced reactions of diaryltetrazoles with carboxylic acids in aqueous solution were investigated. Besides measuring… 
2012
2012
Efficient synthesis of 2,5-disubstituted tetrazoles via the Cu2O-catalyzed aerobic oxidative direct cross-coupling of N-H free tetrazoles with boronic acids.
We present a new protocol that allows for the synthesis of 2,5-disubstituted tetrazoles via the direct coupling of N-H free… 
2010
2010
Direct C-H arylation and alkenylation of 1-substituted tetrazoles: phosphine as stabilizing factor.
Direct arylation and alkenylation of 1-substituted tetrazoles was achieved via Pd catalysis in the presence of CuI and Cs(2)CO(3… 
2010
2010
S1P receptor mediated activity of FTY720 phosphate mimics.
Review
2007
Review
2007
Mapping convulsants’ binding to the GABA-A receptor chloride ionophore: A proposed model for channel binding sites
2007
2007
Synthesis and evaluation of novel heterocyclic MMP inhibitors.
2000
2000
Equilibria of the 5-substituted-1,2-acylated tetrazoles and imidoyl azides
Equilibrium of acylated-5-alkyloxy (aryloxy) tetrazoles and acylated-imidoyl azides was measured by (1)H NMR and/or IR… 
1998
1998
A study of solvent polarity and hydrogen bonding effects on the nitrogen NMR shielding of isomeric tetrazoles and ab initio calculation of the nitrogen shielding of azole systems
High-precision nitrogen NMR shieldings, bulk susceptibility corrected, are reported for the N-methyl derivatives of the two… 
1991
1991
Carboxylic acids and tetrazoles as isosteric replacements for sulfate in cholecystokinin analogues.
A series of analogues of the satiety-inducing peptide cholecystokinin (CCK-8) was prepared in which the sulfated tyrosine… 
1990
1990
N-[(arylmethoxy)phenyl] carboxylic acids, hydroxamic acids, tetrazoles, and sulfonyl carboxamides. Potent orally active leukotriene D4 antagonists of novel structure.
Four series of N-[(arylmethoxy)phenyl] compounds were prepared as leukotriene D4 (LTD4) antagonists. In the hydroxamic acid… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)