Keywords: Oxindoles; Quinolinones; Solid state melt reaction; Isotopic labeling; Mass spectrometry;
مقالات ISI (ترجمه نشده)
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Keywords: Organocatalysis; Superbase; Iminophosphorane; Oxindoles; Hydroxylation;
Keywords: Oxindoles; Allylic alcohols; Palladium; Catalysis; Deacylation;
Keywords: Oxindoles; Isatins; Oxidation; Hyper valent iodine(III);
Keywords: Oxindoles; Analgesia; Antinociception; Pain;
Keywords: 1,4-Benzoquinones; Oxindoles; Enantioselective catalysis; Tandem reaction; Organocatalyst;
Keywords: Metal-free; Diazoamides; Oxindoles; Spirocyclopropanes;
Keywords: Isatin; Organoaluminum; Oxindoles; Catalyst-free conditions;
Keywords: Palladium; Oxidative arylation; Chelation; Oxindoles; Tetrasubstituted olefin;
Design, synthesis and biological evaluation of 1, 4-dihydro indeno[1,2-c] pyrazole linked oxindole analogues as potential anticancer agents targeting tubulin and inducing p53 dependent apoptosis
Keywords: 1, 4-dihydroindeno-[1, 2-c] pyrazole; Oxindoles; Knoevenagel condensation; p53; Apoptosis;
Synthesis of highly substituted 3-arylideneindolin-2-ones
Keywords: Sirtuins; Indolin-2-ones; Oxindoles; 3-Arylideneindolin-2-ones; Cross-coupling;
Bioreduction of the CC double bond with Pseudomonas monteilii ZMU-T17: one approach to 3-monosubstituted oxindoles
Keywords: Bioreduction; Whole cell; Oxindoles; CC double bond; Pseudomonas monteilii ZMU-T17;
First stereospecific total synthesis of (â)-affinisine oxindole as well as facile entry into the C(7)-diastereomeric chitosenine stereochemistry
Keywords: Affinisine oxindole; Oxindoles; Oxindole-rearrangement; Palladium-catalyzed cross coupling; Tetrahydro-β-carbolines;
Synthesis of 3,3-disubstituted oxindoles from anilines nitrosated in situ: a radical-promoted reaction of aromatic amines with N-arylacrylamides
Keywords: Oxindoles; Diazonium salts; Aromatic amine; Arylacrylamide;
A metal-free synthesis of oxindoles by a radical addition-cyclization onto N-arylacrylamides with xanthates
Keywords: Oxindoles; Metal free; Alkenes; Xanthates; Radical; VPOUZFOZLHRGBK-XJZMZMRISA-N; KJNDAWRZQGNHPV-PZYGRECOSA-N; RAVVVNZCRGBNLS-UEVMWXEFSA-N; MGEFKEVCKAPXHV-HJZXTYHSSA-N; ZCCHLWBWWKBNTL-BLTFFBPFSA-N; KFUUOOZJKDLPCI-IREPRJARSA-N; USRCHSZRRKZMSD-DNYRVLSESA-N;
Iron(III) acetylacetonate catalyzed tandem oxidative addition/cyclization of simple amides with alkenes: a convenient process to synthesize 3-amido oxindoles
Keywords: Amides; Iron catalysis; Oxindoles; Tendem CDC reaction; RGGLWBNYNCGYED-PZMINHFJSA-N; VVYVWFABVVUFJK-UHFFFAOYSA-N;
Arylnitration of alkenes by nitration/C-H functionalization cascade using AgNO3 and HOAc
Keywords: Arylnitration; Oxindoles; Dihydroquinolin-2(1H)-ones; C-H functionalization; Alkenes;
Highly regioselective synthesis of 3-alkylthio-2-oxindoles via DABCO-catalyzed allylic α-substitution of Morita-Baylis-Hillman carbonates of isatins with various thiols
Keywords: Oxindoles; DABCO; Allylic sulfuration; MBH carbonates; Thiols;
Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity
Keywords: Oxindoles; Michael addition; Cyclization; Diastereoselectivity; Leishmanicidal activity; Leishmania;
Synthesis of spiroindoline phytoalexin (S)-(â)-spirobrassinin and its unnatural (R)-(+)-enantiomer
Keywords: Indole phytoalexins; Oxindoles; Spirobrassinin; Stereoselectivity; Spirocyclization;
Nucleophilic substitution reaction of Morita-Baylis-Hillman adducts of isatin with X, S, N, and O-nucleophiles: a facile and efficient synthesis of highly functionalized tetrasubstituted alkene appended oxindoles
Keywords: Isatin; Isomerization; Morita-Baylis-Hillman adduct; Tetrasubstituted alkene; Nucleophiles; Oxindoles;
Ultrasound promoted clay catalyzed efficient and one pot synthesis of substituted oxindoles
Keywords: Clay catalyzed reaction; Sonication; Oxindoles
Rhodium(II) acetate-catalyzed stereoselective synthesis, SAR and anti-HIV activity of novel oxindoles bearing cyclopropane ring
Keywords: Oxindoles; Stereoselective synthesis; SAR; NNRTIs; Anti-HIV; MTT assay
A highly efficient synthesis of oxindoles using a functionalized silica gel as support for indium(III) acetylacetonate catalyst in an aqueous-acetonitrile medium
Keywords: Indium(III) acetylacetonate complex; Functionalized; Silica gel; Oxindoles; 13C-CPMAS spectral studies
Tandem Horner-Wadsworth-Emmons/Heck procedures for the preparation of 3-alkenyl-oxindoles: the synthesis of Semaxanib and GW441756
Keywords: Heck; Horner-Wadsworth-Emmons; Phosphonates; Palladium catalysis; Oxindoles; Tandem reactions; Semaxanib; GW441756;
Iridium catalysed C-3 alkylation of oxindole with alcohols under solvent free thermal or microwave conditions
Keywords: Microwave; Ir catalysis; Green chemistry; Regioselective alkylation; Oxindoles;
Total synthesis of (±)-debromoflustramine B and E and (±)-debromoflustramide B based on one-pot intramolecular Ullmann coupling and Claisen rearrangement
Keywords: Oxindoles; Claisen rearrangement; Ullmann coupling; Total synthesis; Pyrrolidinoindoline alkaloids; One-pot reaction;
Structural model of the Plasmodium CDK, Pfmrk, a novel target for malaria therapeutics
Keywords: Plasmodium falciparum; CDK; Pfmrk; Structural model; Homology modelling; Oxindoles; Ligand docking;