# The Journal of Organic Chemistry

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/the-journal-of-organic-chemistry/

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 0022-3263 |
| ISSNs | 0022-3263,1520-6904 |
| OpenAlex ID | https://openalex.org/S205050996 |
| Publisher | American Chemical Society |

## Journal papers

Showing 12 of 27.

- [Catalytic Oxidation of Alkylbenzenes with Molecular Oxygen under Normal Pressure and Temperature by <i>N</i>-Hydroxyphthalimide Combined with Co(OAc)<sub>2</sub>](https://scholariq.org/papers/catalytic-oxidation-of-alkylbenzenes-with-molecular-oxygen-under-normal-pressure/)
- [CF<sub>3</sub> Oxonium Salts, <i>O</i>-(Trifluoromethyl)dibenzofuranium Salts:  In Situ Synthesis, Properties, and Application as a Real CF<sub>3</sub><sup>+</sup> Species Reagent](https://scholariq.org/papers/cf-sub-3-sub-oxonium-salts-i-o-i-trifluoromethyl-dibenzofuranium-salts-in-situ/)
- [Three Rhodamine-Based “Off–On” Chemosensors with High Selectivity and Sensitivity for Fe<sup>3+</sup> Imaging in Living Cells](https://scholariq.org/papers/three-rhodamine-based-off-on-chemosensors-with-high-selectivity-and-sensitivity/)
- [<i>N</i>-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent](https://scholariq.org/papers/i-n-i-trifluoromethylthio-dibenzenesulfonimide-a-shelf-stable-broadly-applicable/)
- [New Method for Trifluoromethylation of Enolate Anions and Applications to Regio-, Diastereo- and Enantioselective Trifluoromethylation](https://scholariq.org/papers/new-method-for-trifluoromethylation-of-enolate-anions-and-applications-to-regio/)
- [Nucleophilic Fluoroalkylation of Epoxides with Fluorinated Sulfones](https://scholariq.org/papers/nucleophilic-fluoroalkylation-of-epoxides-with-fluorinated-sulfones/)
- [Rearrangement Reactions of (Hydroxyphenyl)carbenes](https://scholariq.org/papers/rearrangement-reactions-of-hydroxyphenyl-carbenes/)
- [Additions of PH<sub>3</sub> to Monosubstituted Alkenes of the Formula H<sub>2</sub>CCH(CH<sub>2</sub>)<i><sub>x</sub></i>(CF<sub>2</sub>)<i><sub>y</sub></i>CF<sub>3</sub>:  Convenient, Multigram Syntheses of a Family of Partially Fluorinated Trialkylphosphines with Modulated Electronic Properties and Fluorous Phase Affinities](https://scholariq.org/papers/additions-of-ph-sub-3-sub-to-monosubstituted-alkenes-of-the-formula-h-sub-2-sub/)
- [Gold-Catalyzed Sequential Alkyne Activation: One-Pot Synthesis of NH-Carbazoles via Cascade Hydroarylation of Alkyne/6-Endo-Dig Carbocyclization Reactions](https://scholariq.org/papers/gold-catalyzed-sequential-alkyne-activation-one-pot-synthesis-of-nh-carbazoles/)
- [Manganese-Mediated Reactions in Aqueous Media:  Chemoselective Allylation and Pinacol Coupling of Aryl Aldehydes](https://scholariq.org/papers/manganese-mediated-reactions-in-aqueous-media-chemoselective-allylation-and/)
- [Manganese-Mediated Carbon−Carbon Bond Formation in Aqueous Media:  Chemoselective Allylation and Pinacol Coupling of Aryl Aldehydes](https://scholariq.org/papers/manganese-mediated-carbon-carbon-bond-formation-in-aqueous-media-chemoselective/)
- [Regio- and Diastereoselective Allenylation of Aldehydes in Aqueous Media:  Total Synthesis of (+)-Goniofufurone<sup>1</sup>](https://scholariq.org/papers/regio-and-diastereoselective-allenylation-of-aldehydes-in-aqueous-media-total/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.