Novel non‐toxic and non‐hazardous solvent systems for the chemistry of indoles: use of a sulfone‐containing Brønsted acid
![Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b02303/asset/images/large/ol-2017-023035_0002.jpeg)
Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters
Diels−Alder Approach for the Construction of Halogenated, o-Nitro Biaryl Templates and Application to the Total Synthesis of the Anti-HIV Agent Siamenol | The Journal of Organic Chemistry
Insight into Copper Catalysis: In Situ Formed Nano Cu2O in Suzuki–Miyaura Cross-Coupling of Aryl/Indolyl Boronates | Organic Letters
Novel non‐toxic and non‐hazardous solvent systems for the chemistry of indoles: use of a sulfone‐containing Brønsted acid
Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters
![Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.8b01495/asset/images/medium/ol-2018-01495t_0002.gif)
Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters
![Large Acene Derivatives with B–N Lewis Pair Doping: Synthesis, Characterization, and Application | Organic Letters Large Acene Derivatives with B–N Lewis Pair Doping: Synthesis, Characterization, and Application | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c00033/asset/images/medium/ol2c00033_0007.gif)
Large Acene Derivatives with B–N Lewis Pair Doping: Synthesis, Characterization, and Application | Organic Letters
Preparation of Polyfunctional Aryl Azides from Aryl Triazenes. A New Synthesis of Ellipticine, 9-Methoxyellipticine, Isoellipticine, and 7-Carbethoxyisoellipticine | The Journal of Organic Chemistry
![Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF](https://i1.rgstatic.net/ii/profile.image/1171498018574338-1656318301302_Q64/Melina-Vogt.jpg)
Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF
![Pd(II)-Catalyzed Synthesis of Alkylidene Phthalides via a Decarbonylative Annulation Reaction | Organic Letters Pd(II)-Catalyzed Synthesis of Alkylidene Phthalides via a Decarbonylative Annulation Reaction | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.9b00726/asset/images/medium/ol-2019-00726k_0009.gif)
Pd(II)-Catalyzed Synthesis of Alkylidene Phthalides via a Decarbonylative Annulation Reaction | Organic Letters
Bio- and Medicinally Compatible α-Amino-Acid Modification via Merging Photoredox and N-Heterocyclic Carbene Catalysis | Organic Letters
![Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.8b01495/asset/images/medium/ol-2018-01495t_0006.gif)
Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes | Organic Letters
Pd(II)-Catalyzed Synthesis of Alkylidene Phthalides via a Decarbonylative Annulation Reaction | Organic Letters
![Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF](https://i1.rgstatic.net/ii/profile.image/1179148819136513-1658142394069_Q64/Kandikere-Ramaiah.jpg)
Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF
Large Acene Derivatives with B–N Lewis Pair Doping: Synthesis, Characterization, and Application | Organic Letters
![Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF](https://i1.rgstatic.net/ii/profile.image/1136654353993729-1648010924430_Q64/Seijiro-Matsubara.jpg)
Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1 H -indol-3-yl)-9 H -carbazole | Request PDF
![Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b02303/asset/images/medium/ol-2017-023035_0007.gif)
Gold-Catalyzed Synthesis of 1-(Indol-3-yl)carbazoles: Selective 1,2-Alkyl vs 1,2-Vinyl Migration | Organic Letters
![Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1H-indol-3-yl)-9H-carbazole - ScienceDirect Metal-Free C–H Functionalization and Aromatization Sequence for the Synthesis of 1-(Indol-3-yl)carbazoles and Total Synthesis of 7-Bromo-1-(6-bromo-1H-indol-3-yl)-9H-carbazole - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1523706021042085-ol-2018-03848t_0008.jpg)