Results 91 to 100 of about 1,205 (207)
The synthesis of spirooxindoles bearing tetrahydro-4H-cyclopenta[b]furan framework was established starting from isatin-derived aldehydes and 2 equiv of 1,3-dicarbonyl compounds involving a piperidine-catalyzed ABB′ three-component domino process. This
Muthu Karuppasamy +15 more
core +2 more sources
In the current medical era, spirooxindole motif stands out as a privileged heterospirocyclic scaffold that represents the core for a wide range of bioactive naturally isolated products (such as Strychnofoline and spirotryprostatins A and B) and synthetic
Sara T. Al-Rashood +7 more
doaj +1 more source
Taking into account the postulated reaction mechanism for the organocatalytic epoxidation of electron-poor olefins developed by our laboratory, we have investigated the key factors able to positively influence the H-bond network installed inside the ...
Martina Miceli +9 more
doaj +1 more source
This PhD work concerns the use of sulfinate anions (RSO2–) as catalysts, within sulfinate/ammonium ion pairs RSO2/NR4, in organocatalyzed annelation processes leading to biologically relevant cyclopentene spirooxindoles. The methodologies involve anionic
Martin, Victorien
core
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.
R. Madhavachary +5 more
core +1 more source
Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization
A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins and 1,3-dicarbonyl compounds with pyridine derivatives is reported. The reactions provided good to excellent yields.
Chunhui Dai +2 more
doaj +1 more source
Les travaux décrits dans cette thèse ont pour fil conducteur l’exploitation des paires d’ions sulfinate/ammonium RSO2–/+NR4, à travers des réactions d’annélation permettant d’accéder à des cyclopentènes spirooxindoles.
Martin, Victorien
core
The development of a versatile new one pot, catalyst free, multicomponent-tandem strategy for assembly of spirooxindole-indazolones and spirooxindole-pyrazolines is described.
Swastika Singh +4 more
openaire +1 more source
Selective Synthesis of Spirooxindoles by an Intramolecular Heck–Mizoroki Reaction
We report a highly diastereoselective synthesis of cydopentene-spirooxindole derivatives via an intramolecular Heck-Mizoroki reaction using aryl bromides as precursors. The reactions were performed under dry conditions or in a DMF-water system.
Wetzel, Alexander, +13 more
core +1 more source
Dehydrative Transformation of Spirooxindoles to Pyrido[2,3‑b]indoles via POCl3
A two-step one-pot efficient synthesis of pyrido[2,3-b]indoles via reaction between isatin, α-amino acid, and dipolarophile has been developed. The initial 1,3-dipolar cycloaddition between the reactants that is performed in the presence of either CuI ...
Aritra Ghosh (581661) +5 more
core +2 more sources

