Results 1 to 10 of about 2,239,206 (182)

Three-component radical homo Mannich reaction [PDF]

open access: yesNature Communications, 2021
Due to the ionic nature of its mechanism, the Mannich reaction can only use non-enolizable aldehydes as substrates. Here, the authors expand the scope of the classical Mannich reaction to enolizable aldehydes by employing a radical process resulting in a
Shuai Shi   +5 more
doaj   +3 more sources

Photoinduced Synthesis of Sulfonyl-Containing Phosphorothioates via a Three-Component Reaction [PDF]

open access: yesMolecules, 2023
Both sulfonyl and phosphorothioate are important privileged structural motifs which are widely presented in pharmaceuticals and agrochemicals. Herein, we describe an efficient approach to synthesizing sulfonyl-containing phosphorothioates by merging ...
Xianda Wu   +5 more
doaj   +2 more sources

Three-Component Reaction of 3-Arylidene-3H-Indolium Salts, Isocyanides, and Alcohols [PDF]

open access: yesFrontiers in Chemistry, 2019
A novel isocyanide-based multicomponent synthesis of alkyl aryl(indol-3-yl)acetimidates has been established. Starting from aryl(indol-3-yl)methylium tetrafluoroborates, aromatic isocyanides and alcohols, the imidates were obtained in moderate to very ...
Nikita E. Golantsov   +6 more
doaj   +2 more sources

Catalytic Three‐Component Ugi Reaction [PDF]

open access: yesAngewandte Chemie International Edition, 2008
Perfect atom economy characterizes a novel catalytic three‐component Ugi reaction (see example). Different α‐amino amides are formed in good yields from aldehydes, primary amines, and isocyanides in the presence of phenyl phosphinic acid as the catalyst. The products will be useful for the synthesis of α‐amino acid derivatives and in diversity‐oriented
Pan, S., List, B.
openaire   +3 more sources

Catalytic Asymmetric Three‐Component Acyl‐Strecker Reaction. [PDF]

open access: yesChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Pan, S., List, B.
openaire   +3 more sources

DFT Studies on the Stereoselective Three-Component Ugi Reaction

open access: yesOrbital: The Electronic Journal of Chemistry, 2019
Mechanism and stereochemistry of three component Ugi reaction (3C-Ugi) were studied theoretically based on DFT calculations. Structures of reagents, products, intermediates, and transition states were optimized at M062X/6-31+g(d,p) level of theory in gas
Elaheh Sadat Sharifzadeh   +1 more
doaj   +3 more sources

Novel pH-sensitive catechol dyes synthesised by a three component one-pot reaction

open access: yesFrontiers in Chemistry, 2023
The synthesis and characterisation of new dyes based on indolizines bearing catechol groups in their structure is presented. The preparation was carried out through a simple three component one-pot reaction promoted by CuNPs/C, between pyridine-2 ...
Juan José Calmels   +7 more
doaj   +1 more source

Stabilization of gold nanoparticles on copper ferrrite and its application as bimetallic and magnetically recyclable catalyst for preparation of propargylamines [PDF]

open access: yesشیمی کاربردی روز, 2018
In this report for the first time, gold nanoparticles were supported and stabilized on copper ferrite nanoparticles (CuFe2O4 NPs) and obtained compound was characterized by different techniques such as transmission electron microscopy (TEM), X-ray ...
Mohammad Gholinejad   +3 more
doaj   +1 more source

Various Synthetic Pathways for the Synthesis of 3,4-Disubstituted Isoxazole by One Pot Multicomponent Reaction

open access: yesOrbital: The Electronic Journal of Chemistry, 2020
Isoxazole is a five membered heterocyclic compound which is an azole with an oxygen atom next to nitrogen. The substituted isoxazole derivatives show various biological activities like antimicrobial, antiviral, anti-inflammatory, antioxidant, anticancer ...
Parul Setia, Ruchi Bharti, Renu Sharma
doaj   +3 more sources

Home - About - Disclaimer - Privacy