Results 1 to 10 of about 4,626 (187)

Sulfate radical anion-induced benzylic oxidation of N-(arylsulfonyl)benzylamines to N-arylsulfonylimines [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2023
A mild, operationally convenient, and practical method for the synthesis of synthetically useful N-arylsulfonylimines from N-(arylsulfonyl)benzylamines using K2S2O8 in the presence of pyridine as a base is reported herein. In addition, a “one-pot” tandem
Joydev K. Laha   +2 more
doaj   +2 more sources

Bio-inspired manganese-catalyzed deaminative hydroxylation of benzyl amines to corresponding alcohols [PDF]

open access: yesNature Communications
Direct conversion of amines to corresponding alcohols is challenging even under harsh reaction conditions. Inspired by enzymatic transamination, we present a transamination borrowing-hydrogen strategy that enables the direct and selective Mn-catalyzed ...
Jiale Ji   +6 more
doaj   +2 more sources

Direct asymmetric α C(sp 3 )‒H alkylation of benzylamines with MBH acetates enabled by bifunctional pyridoxal catalysts [PDF]

open access: yesNature Communications
Organocatalytic allylic substitution of Morita-Baylis-Hillman (MBH) adducts is widely regarded as one of the most powerful transformations in organic synthesis.
Jiayao Chen   +7 more
doaj   +2 more sources

Electrocatalytic hydrogenation of cyanoarenes, nitroarenes, quinolines, and pyridines under mild conditions with a proton-exchange membrane reactor [PDF]

open access: yesBeilstein Journal of Organic Chemistry
An electrocatalytic hydrogenation of cyanoarenes, nitroarenes, quinolines, and pyridines using a proton-exchange membrane (PEM) reactor was developed. Cyanoarenes were then reduced to the corresponding benzylamines at room temperature in the presence of ...
Koichi Mitsudo   +6 more
doaj   +2 more sources

Deaminative coupling of benzylamines and arylboronic acids. [PDF]

open access: yesChem Sci, 2023
A metal-free deaminative coupling of non-prefunctionalised benzylamines and arylboronic acids is reported.
Sirvinskaite G   +2 more
europepmc   +4 more sources

NiH-catalyzed asymmetric hydroarylation of N-acyl enamines to chiral benzylamines

open access: yesNature Communications, 2021
Chiral benzylamines are found in many pharmacologically active molecules. Here, the authors report an enantio- and regio-selective reductive hydroarylation of N-acyl enamines with a NiH/chiral bis-imidazoline catalytic system affording a range of ...
Yuli He   +3 more
doaj   +1 more source

Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines

open access: yesMolecules, 2022
We developed a straightforward synthetic route to pharmacologically important 1,5-substituted pyrrolidin-2-ones from donor–acceptor cyclopropanes bearing an ester group as one of the acceptor substituents.
Maksim A. Boichenko   +9 more
doaj   +1 more source

Benzylamines as highly potent inhibitors of the sterol biosynthesis pathway in Leishmania amazonensis leading to oxidative stress and ultrastructural alterations

open access: yesScientific Reports, 2022
Leishmaniasis is a neglected disease caused by protozoan parasites of the Leishmania genus. Benzylamines are a class of compounds selectively designed to inhibit the squalene synthase (SQS) that catalyzes the first committed reaction on the sterol ...
Sara Teixeira de Macedo-Silva   +6 more
doaj   +1 more source

Alkaloids Modulate the Functioning of Ion Channels Produced by Antimicrobial Agents via an Influence on the Lipid Host

open access: yesFrontiers in Cell and Developmental Biology, 2020
It is widely recognized that an alteration in membrane physical properties induced by the adsorption of various drugs and biologically active compounds might greatly affect the functioning of peptides and proteins embedded in the membrane, in particular ...
Svetlana S. Efimova   +2 more
doaj   +1 more source

Benzobicyclo[3.2.1]octene Derivatives as a New Class of Cholinesterase Inhibitors

open access: yesMolecules, 2020
A library of amine, oxime, ether, epoxy and acyl derivatives of the benzobicyclo[3.2.1]octene were synthesized and evaluated as inhibitors of both human acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).
Tena Čadež   +6 more
doaj   +1 more source

Home - About - Disclaimer - Privacy