Results 111 to 120 of about 38,452 (298)
Selective C(sp2)–H Halogenation of “Click” 4‑Aryl-1,2,3-triazoles
Selective bromination reactions of “click compounds” are described. Electron-neutral and electron-deficient arenes selectively undergo unprecedented Pd-catalyzed C–H ortho-halogenations assisted by simple triazoles as modular directing groups, whereas ...
Asier Goitia (3728104) +2 more
core +1 more source
The regioselective and enantioselective intermolecular sp3 C–H functionalization of silicon-substituted alkanes was accomplished using Rh2(S-NTTL)4 with readily available 1-sulfonyl-1,2,3-triazoles as carbene precursors.
Zachary J. Garlets (2734693) +1 more
core +1 more source
In search of more potent new antitubercular agents, a library of novel piperazine tethered dimeric 1,2,3-triazoles were designed by assembling 1,2,3-triazoles and piperazine in a single molecular architectural framework.
Jaiprakash N. Sangshetti (4842510) +6 more
core +1 more source
We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer +6 more
wiley +1 more source
Synthesis, characterization and thermogravimetric study of Cu(II) adducts with 3- and 4-amino-1,2,4-triazole, 2-mercaptothiazoline and 2-mercaptopyridine [PDF]
The adducts CuCl2·(3amt), CuCl2·2(3amt)·2H2O, CuCl2·3(3amt), CuCl2·(4amt), CuCl2·2(4amt), CuCl2·3(4amt)·2H2O, CuCl2·(2mct)·H2O, CuCl2·2(2mct)·2.5H2O, CuCl2·3(2mct)·2H2O, CuCl2·(2mcp) and CuCl2·2(2mcp)·H2O, where 3-amino-1,2,4-triazole = 3amt, 4-amino-1,2,
MOAMEN S. REFAT, ROBSON F. DE FARIAS
doaj
ZINClick v.18: Expanding Chemical Space of 1,2,3-Triazoles
In the last years, we have investigated the click-chemical space covered by molecules containing the triazole ring and generated a database of 1,2,3-triazoles called ZINClick, starting from literature-reported alkynes and azides synthesizable in no more ...
Levré, Doriana +11 more
core +1 more source
Triazole-based STING inhibitors
Aberrant activation of the DNA sensing cGAS-STING pathway has been implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS), systemic lupus erythematosus (SLE), and autoinflammatory disorders such as Aicardi-Goutières syndrome (AGS) and STING-associated vasculopathy with onset in infancy (SAVI). Consequently, considerable efforts have been
Singh, Anju +9 more
openaire +2 more sources
Activation of Metal Complexes With Ultrasound Waves for Targeted Anticancer Therapy
Ultrasound enables non‐invasive activation of metal‐based therapeutics deep within tumors. Acoustic cavitation can drive sonodynamic reactive oxygen species generation or mechanochemical metal–ligand bond dissociation, enabling controlled release of bioactive payloads.
Félix Grosjean +3 more
wiley +1 more source
A novel relay Rh (II)/cobaloxime (III) dual catalysis strategy has been developed for the stereoselective synthesis of indolyl spiroindanones from readily accessible N-sulfonyl-1,2,3-triazoles.
Hongbin Zhai (1457509) +7 more
core +1 more source
Synthesis of 1,2,3-triazoles and applications in the synthesis of BODIPY triazoles
The 1,2,3-triazole ring is an important heterocycle which has found wide applications due to its interesting properties. Mainly due to the advent of the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction, 1,2,3-triazoles are nowadays unavoidable in the chemical literature. In the past decade, the development of transition metal-free synthetic
openaire +2 more sources

