Results 11 to 20 of about 4,664 (217)

Aqueous and Surfactant-Free Synthesis of Nanoscale Covalent Organic Frameworks. [PDF]

open access: yesAngew Chem Int Ed Engl
We report an aqueous, surfactant‐free, and versatile synthesis method for imine‐linked nanoCOFs incorporating porphyrin units, with tunable size and morphology. The resulting nanoCOFs exhibit excellent aqueous dispersibility, strong light absorption, and significantly enhanced photocatalytic activity.
Kong X   +4 more
europepmc   +3 more sources

Mechanochemical Synthesis of Fluorinated Imines

open access: yesMolecules, 2022
A number of imines, including 12 new compounds, previously not reported in the literature, derived from variously fluorinated benzaldehydes and different anilines or chiral benzylamines were synthesized by a solvent-free mechanochemical method, which was
Karolina Ciesielska   +3 more
doaj   +1 more source

Metal-Organic Framework/Organocatalyst Combinations as Powerful Multicatalytic Systems for Aerobic Oxidations. [PDF]

open access: yesAngew Chem Int Ed Engl
A multicatalytic strategy based on the simple combination of metal‐organic frameworks (MOFs) and organocatalysts is able to mediate challenging aerobic oxidation reactions. The use of earth‐abundant MOFs and commercially available (hydro)quinone co‐catalysts greatly simplify the generation of powerful multicatalytic systems, opening the door for the ...
Arango-Daza JC   +5 more
europepmc   +3 more sources

The reaction of arylmethyl isocyanides and arylmethylamines with xanthate esters: a facile and unexpected synthesis of carbamothioates

open access: yesBeilstein Journal of Organic Chemistry, 2020
An unexpected formation of carbamothioates by a sodium hydride-mediated reaction of arylmethyl isocyanides with xanthate esters in DMF is reported. The products thus obtained were compared with the carbamothioates obtained by the sodium hydride-mediated ...
Narasimhamurthy Rajeev   +10 more
doaj   +1 more source

Design of Two Alternative Routes for the Synthesis of Naftifine and Analogues as Potential Antifungal Agents

open access: yesMolecules, 2018
Two practical and efficient approaches have been implemented as alternative procedures for the synthesis of naftifine and novel diversely substituted analogues 16 and 20 in good to excellent yields, mediated by Mannich-type reactions as the key step of ...
Rodrigo Abonia   +8 more
doaj   +1 more source

An Electrochemical Way to Generate Amphiphiles from Hydrazones for the Synthesis of 1,2,4‐Triazole Scaffold Cyclic Compounds

open access: yesChemistryOpen, 2022
An electro‐oxidative cyclization pathway in which hydrazones are selected as starting materials to generate amphiphiles by reacting with benzylamines and benzamides was reported.
Wangyu Li   +5 more
doaj   +1 more source

The catalytic activity of a cyclometalated ruthenium(III) complex for aerobic oxidative dehydrogenation of benzylamines [PDF]

open access: yes, 2011
journal ...
Aiki Shota   +4 more
core   +1 more source

Novel chemoenzymatic oxidation of amines into oximes based on hydrolase-catalysed peracid formation [PDF]

open access: yes, 2017
The efficient transformation of benzylamines into the corresponding oximes has been described by means of a chemoenzymatic process.
Gotor Fernández, Vicente   +3 more
core   +2 more sources

Allylamines, Benzylamines, and Fungal Cell Permeability: A Review of Mechanistic Effects and Usefulness against Fungal Pathogens

open access: yesMembranes, 2022
Allylamines, naftifine and terbinafine, and the benzylamine, butenafine, are antifungal agents with activity on the fungal cell membrane. These synthetic compounds specifically inhibit squalene epoxidase, a key enzyme in fungal sterol biosynthesis.
Dalal Hammoudi Halat   +3 more
doaj   +1 more source

Aerobic oxidative dehydrogenation of benzylamines catalyzed by a cyclometalated ruthenium complex [PDF]

open access: yes, 2010
The ruthenium(III) complex bearing phenylpyridine as a cyclometalated ligand serves as an efficient catalyst for the aerobic oxidative dehydrogenation of benzylamines to the corresponding benzonitriles under mild ...
Koizumi Take-aki   +3 more
core   +1 more source

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