Compounds > 2-oxindole
Page last updated: 2024-08-24

2-oxindole and piperidines

2-oxindole has been researched along with piperidines in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Gallagher, T; Haddow, MF; Hirschhäuser, C; Parker, JS; Perry, MW1
Basiri, A; Kia, Y; Kumar, RS; Murugaiyah, V; Osman, H; Perumal, S; Razak, IA1
Cui, HL; Han, B; He, G; He, XH; Huang, H; Huang, W; Peng, C; Yang, L; Yang, MC1
Amrutha Krishnan, AV; Bharitkar, YP; Hazra, A; Mandal, R; Natarajan, R; Ravichandiran, V; Samanta, J; Singh, M1

Other Studies

4 other study(ies) available for 2-oxindole and piperidines

ArticleYear
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
    Organic letters, 2012, Sep-21, Volume: 14, Issue:18

    Topics: Aniline Compounds; Catalysis; Indoles; Lactams; Molecular Structure; Oxindoles; Piperidines; Pyrrolidines; Spiro Compounds; Stereoisomerism

2012
A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole-pyrrolizine-piperidine hybrids.
    Bioorganic & medicinal chemistry letters, 2013, May-15, Volume: 23, Issue:10

    Topics: Butyrylcholinesterase; Cholinesterase Inhibitors; Cholinesterases; Cyclization; Dose-Response Relationship, Drug; Indoles; Models, Molecular; Molecular Structure; Oxindoles; Piperidines; Pyrroles; Spiro Compounds; Stereoisomerism; Structure-Activity Relationship

2013
Organocatalytic Asymmetric Synthesis of Spiro-oxindole Piperidine Derivatives That Reduce Cancer Cell Proliferation by Inhibiting MDM2-p53 Interaction.
    Organic letters, 2017, 12-15, Volume: 19, Issue:24

    Topics: Antineoplastic Agents; Apoptosis; Binding Sites; Catalysis; Cell Proliferation; Humans; MCF-7 Cells; Molecular Dynamics Simulation; Oxindoles; Piperidines; Proto-Oncogene Proteins c-mdm2; Spiro Compounds; Stereoisomerism; Tumor Suppressor Protein p53

2017
Azomethine ylide cycloaddition: a versatile tool for preparing novel pyrrolizidino-spiro-oxindolo hybrids of the doubly conjugated alkamide piperine.
    Molecular diversity, 2020, Volume: 24, Issue:3

    Topics: Alkaloids; Azo Compounds; Benzodioxoles; Cycloaddition Reaction; Models, Molecular; Molecular Conformation; Oxindoles; Piperidines; Polyunsaturated Alkamides; Pyrroles; Spiro Compounds; Stereoisomerism; Thiosemicarbazones

2020