Results 11 to 20 of about 1,875 (207)

Synthesis of Polyfunctionalized Amino Furans with Long Conjugated Aromatic Systems Using Nucleophilic Aromatic Isocyanide [PDF]

open access: yesE-Journal of Chemistry, 2012
Polyfunctionalized amino furans with long conjugated aromatic systems have been synthesized by three component reaction of aldehydes, acetylenic esters and aromatic nucleophilic isocyanide.
Mohammad Qandalee   +3 more
doaj   +2 more sources

Pd/C-Catalyzed Hydrogenation of CF<sub>3</sub>-, CF<sub>2</sub>H-, and CF<sub>2</sub>CO<sub>2</sub>Et-containing Pyridines: A Robust Method for Highly Functionalized containing Piperidines. [PDF]

open access: yesAngew Chem Int Ed Engl
A robust and efficient method to access diversely functionalized fluorinated piperidines was developed. The approach features the hydrogenation of polysubstituted pyridines bearing CF3, CF2H, and CF2CO2Et substituents using an inexpensive, readily available heterogeneous Pd/C catalyst under air‐ and moisture‐tolerant conditions, offering an appealing ...
Charvillat T   +7 more
europepmc   +2 more sources

(E)-4-Oxo-3,4-dihydroquinazoline-2-carbaldehyde Oxime

open access: yesMolbank, 2021
Reaction of 4-oxo-3,4-dihydroquinazoline-2-carbaldehyde with hydroxylamine hydrochloride (1.1 equiv) in the presence of K2CO3 (1 equiv) gave (E)-4-oxo-3,4-dihydroquinazoline-2-carbaldehyde oxime (8) in 58% yield.
Andreas S. Kalogirou   +2 more
doaj   +1 more source

Access to Polyfunctionalized Diquinanes, Hydrindanes, and Decalines via TiCl4 Promoted Michael–Aldol and Baylis–Hillman Reactions

open access: yes, 2016
The addition of 0.5 equiv of TiCl4 to (cyclo)alkanones tethered to α,β-unsaturated ketones afforded polyfunctionalized diquinanes, hydrindanes, and decalines.
Alexis Jaunet (1867663)   +4 more
core   +9 more sources

Reactions of 4H-1,2,6-Thiadiazine Sulfides

open access: yesMolbank, 2022
3,5-Dichloro-4H-1,2,6-thiadiazin-4-one reacts with benzo[d]thiazole-2-thiol (1 equiv) and triethylamine (1 equiv) to give 3-(benzo[d]thiazol-2-ylthio)-5-chloro-4H-1,2,6-thiadiazin-4-one in 71% yield.
Andreas S. Kalogirou   +1 more
doaj   +1 more source

Contilisant+Tubastatin A hybrids, as new multi-target-directed polyfunctionalized indole derivatives able to inhibit histone deacetylase/cholinesterase/monoamine oxidase enzymes, and modulate histamine 3/sigma 1/5-HT6/dopamine 3 receptors for the treatment of cancer [PDF]

open access: yes, 2023
Herein we describe the design and synthesis of Contilisant+Tubastatin A hybrids as polyfunctionalized indole derivatives for the treatment of a broad diversity of cancers, such as glioblastoma.
Ander , Matheu   +10 more
core   +2 more sources

Reaction of 4,5-Dichloro-1,2,3-dithiazolium Chloride with 2-(Phenylsulfonyl)acetonitrile

open access: yesMolbank, 2022
The reaction of 4,5-dichloro-1,2,3-dithiazolium chloride with 2-(phenylsulfonyl)acetonitrile (1 equiv) in the presence of pyridine (2 equiv) gave S-(3-chloro-5-cyanoisothiazol-4-yl)benzenesulfonothioate and (Z)-2-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)-2-
Konstantinos Plakas   +3 more
doaj   +1 more source

2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile

open access: yesMolbank, 2021
The reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized.
Andreas S. Kalogirou   +1 more
doaj   +1 more source

Methyl 3-Bromo-5-carbamoylisothiazole-4-carboxylate

open access: yesMolbank, 2023
Reaction of methyl 3-bromo-5-cyanoisothiazole-4-carboxylate with conc. H2SO4 gave methyl 3-bromo-5-carbamoylisothiazole-4-carboxylate in 93% yield. The compound was fully characterized.
Andreas S. Kalogirou   +1 more
doaj   +1 more source

Fluorinated and Non-Fluorinated 1,4-Diarylpyrazoles via MnO2-Mediated Mechanochemical Deacylative Oxidation of 5-Acylpyrazolines

open access: yesMolecules, 2022
A solvent-free two-step synthesis of polyfunctionalized pyrazoles under ball-milling mechanochemical conditions was developed. The protocol comprises (3 + 2)-cycloaddition of in situ generated nitrile imines and chalcones, followed by oxidation of the ...
Greta Utecht-Jarzyńska   +2 more
doaj   +1 more source

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