Results 91 to 100 of about 1,205 (207)

Diastereoselective ABB′ Three-Component Synthesis of Highly Functionalized Spirooxindoles Bearing Five Consecutive Asymmetric Carbons

open access: yes, 2019
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

Antitumor properties of certain spirooxindoles towards hepatocellular carcinoma endowed with antioxidant activity

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2020
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

Asymmetric Synthesis of Spirooxindoles via Nucleophilic Epoxidation Promoted by Bifunctional Organocatalysts

open access: yesMolecules, 2018
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

Nouvelles voies d'accès aux clyclopentènes spirooxindoles : activation d'allényl sulfones par des paires d'ions sulfinate ammonium

open access: yes, 2020
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

open access: yes, 2013
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

open access: yesBeilstein Journal of Organic Chemistry, 2012
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

Original accesses to cyclopentene spirooxindoles : activation of allenyl sulfones by sulfinate ammonium ion pairs

open access: yes, 2020
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  

Catalyst free, multicomponent-tandem synthesis of spirooxindole-indazolones and spirooxindole-pyrazolines: a glycerol mediated green approach

open access: yesRSC Advances, 2015
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

open access: yes, 2017
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

open access: yes, 2019
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

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