Results 11 to 20 of about 6,074 (218)
Electrostatic Activation of Tetrazoles [PDF]
The Journal of Organic Chemistry, 2020 Photoactivation of tetrazoles to form nitrile imines primed for 1,3-dipolar cycloaddition reactions is of widespread utility in chemistry. In contrast, the corresponding thermal reactions usually possess prohibitively high barriers and have garnered significantly less attention.
Vincent Doan +2 more
openaire +5 more sources
Multi-Gram Synthesis of Enantiopure 1,5-Disubstituted Tetrazoles Via Ugi-Azide 3-Component Reaction
Molecules, 2018 Tetrazoles have been widely studied for their biological properties. An efficient route for large-scale synthesis of 1,5-disubstituted tetrazoles (1,5-DTs) is presented.
Pietro Capurro +4 more
doaj +2 more sources
TADF-Active Tetrazole Luminophores for Visible-Light Functionalization of Nanoparticles and Surfaces. [PDF]
Angew Chem Int Ed EnglA series of tetrazoles are reported that undergo 1,3‐dipolar cycloadditions with alkene and alkyne substrates, generating (dihydro)pyrazole products that exhibit thermally activated delayed fluorescence (TADF). The “photo‐click” reactivity of these tetrazoles is leveraged to functionalize nanoparticles and surfaces with TADF‐active chromophores ...
Hojo R +11 more
europepmc +3 more sources
Tetrazoles: a new class of compound for crystallization modification [PDF]
, 2010 Tetrazoles are a class of organic compound often used as carboxylic acid analogues. This analogous behaviour is shown to extend to crystallization modification, that is, tetrazoles are also able to influence crystal growth and morphology although in a ...
Franca Jones (1838584) +3 more
core +2 more sources
Alkylation of 5‑Substituted 1H‑Tetrazoles via the Diazotization of Aliphatic Amines
, 2021 A new alkylation reaction of monosubstituted tetrazoles via the diazotization of aliphatic amines is reported. This method enables preferential formation of 2,5-disubstituted tetrazoles. A one-pot 1,3-dipolar cycloaddition/diazotization sequence starting
Guillaume Reynard (11286297) +1 more
core +2 more sources
6-(Tetrazol-5-yl)-7-aminoazolo[1,5-a]pyrimidines as Novel Potent CK2 Inhibitors
Molecules, 2022 In this work, we describe the design, synthesis, and structure-activity relationship of 6-(tetrazol-5-yl)-7-aminoazolo[1,5-a]pyrimidines as inhibitors of Casein kinase 2 (CK2).
Grigoriy V. Urakov +6 more
doaj +1 more source
Materials Research Express, 2021 The current research represents a facile and competent methodology in the development of a novel magnetic nanocatalyst. This composite was synthesized by immobilizing La on Fe _3 O _4 nanoparticles pre-functionalized with tetrahydroharman-3-carboxylic ...
Taiebeh Tamoradi +3 more
doaj +1 more source
Molbank, 2022 The Diels–Alder reaction of ethyl 3-(1-phenyl-1H-tetrazol-5-yl-1,2-diaza-1,3-butadiene-1-carboxylate with 2-acetyl-6-methyl-2,3-dihydro-4H-pyran (methyl vinyl ketone dimer) regioselectively afforded the corresponding 3-(tetrazol-5-yl)-hexahydro-7H-pyrano[
Susana M. M. Lopes +3 more
doaj +1 more source
Chemical Communications, 2020 We surprisingly found that combining the substrates of Ugi tetrazole reaction gives two different constitutional isomeric Ugi products A and B. A is the expected classical Ugi products whereas B is an isomeric product (‘atypical Ugi’).
Eman M. M. Abdelraheem +6 more
openaire +5 more sources
Mechanistic DFT Study of 1,3-Dipolar Cycloadditions of Azides with Guanidine
Molecules, 2023 Density functional calculations SMD(chloroform)//B3LYP/6-311+G(2d,p) were employed in the computational study of 1,3-dipolar cycloadditions of azides with guanidine.
Ivana Antol +2 more
doaj +1 more source