Synthesis of 4‑Hydroxyindolin-2-ones\nvia Phosphoric\nAcid-Mediated Annulation of β‑Nitrostyrenes with 1,3-Cyclohexanedione

The efficient synthesis of 4-hydroxy-3-arylindolin-2-ones\nvia phosphoric\nacid-mediated annulation of various β-nitrostyrenes and 1,3-cyclohexanedione\nis described. This annulation reaction gives a practical method for\naffording a diverse set of oxindoles, having simple experimentation,\n readily available starting materials, and very good yields. Additionally,\nsubstituted 1,3-cyclohexanediones under the same conditions afforded\ntetrahydrobenzofuran oxime compounds.

Publication Details

Journal
Figshare
Published
2024-11-12
DOI
https://doi.org/10.1021/acs.joc.4c01910.s001
Primary Topic
Synthesis of heterocyclic compounds
Type
article
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article

Synthesis of 4‑Hydroxyindolin-2-ones\nvia Phosphoric\nAcid-Mediated Annulation of β‑Nitrostyrenes with 1,3-Cyclohexanedione

Figshare
Synthesis of heterocyclic compounds
article

Synthesis of 4‑Hydroxyindolin-2-ones\nvia Phosphoric\nAcid-Mediated Annulation of β‑Nitrostyrenes with 1,3-Cyclohexanedione

article en

Abstract

The efficient synthesis of 4-hydroxy-3-arylindolin-2-ones\nvia phosphoric\nacid-mediated annulation of various β-nitrostyrenes and 1,3-cyclohexanedione\nis described. This annulation reaction gives a practical method for\naffording a diverse set of oxindoles, having simple experimentation,\n readily available starting materials, and very good yields. Additionally,\nsubstituted 1,3-cyclohexanediones under the same conditions afforded\ntetrahydrobenzofuran oxime compounds.

Figshare
Openalex Percentile: Top 76%
Synthesis of heterocyclic compounds
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Synthesis of 4‑Hydroxyindolin-2-ones\nvia Phosphoric\nAcid-Mediated Annulation of β‑Nitrostyrenes with 1,3-Cyclohexanedione · Figshare (2024) | TGRS Research Map | TGRS