![Molecules | Free Full-Text | 4,5,6,7-Tetrahydroindol-4-Ones as a Valuable Starting Point for the Synthesis of Polyheterocyclic Structures | HTML Molecules | Free Full-Text | 4,5,6,7-Tetrahydroindol-4-Ones as a Valuable Starting Point for the Synthesis of Polyheterocyclic Structures | HTML](https://www.mdpi.com/molecules/molecules-26-04596/article_deploy/html/images/molecules-26-04596-sch024.png)
Molecules | Free Full-Text | 4,5,6,7-Tetrahydroindol-4-Ones as a Valuable Starting Point for the Synthesis of Polyheterocyclic Structures | HTML
![Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-022-09799-1/MediaObjects/41598_2022_9799_Fig4_HTML.png)
Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports
![Recent advances in spirocyclization of indole derivatives - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00508C Recent advances in spirocyclization of indole derivatives - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00508C](https://pubs.rsc.org/image/article/2018/CS/c7cs00508c/c7cs00508c-s23_hi-res.gif)
Recent advances in spirocyclization of indole derivatives - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00508C
![Generic structure of indole-based synthetic cannabinoids (adapted from... | Download Scientific Diagram Generic structure of indole-based synthetic cannabinoids (adapted from... | Download Scientific Diagram](https://www.researchgate.net/profile/Brandon-Presley/publication/326374644/figure/fig4/AS:658631901081600@1534041490340/Generic-structure-of-indole-based-synthetic-cannabinoids-adapted-from-87.png)
Generic structure of indole-based synthetic cannabinoids (adapted from... | Download Scientific Diagram
![Synthesis of the Azocino[cd]indole Framework through Pd‐Catalyzed Intramolecular Acetylene Hydroarylation - Peshkov - 2011 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of the Azocino[cd]indole Framework through Pd‐Catalyzed Intramolecular Acetylene Hydroarylation - Peshkov - 2011 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/64d0fce9-3360-4b5e-94c6-97bb8fa6167d/mfig000.jpg)
Synthesis of the Azocino[cd]indole Framework through Pd‐Catalyzed Intramolecular Acetylene Hydroarylation - Peshkov - 2011 - European Journal of Organic Chemistry - Wiley Online Library
![Tandem Nenitzescu Reaction/Nucleophilic Aromatic Substitution to Form Novel Pyrido Fused Indole Frameworks - Singh - 2021 - European Journal of Organic Chemistry - Wiley Online Library Tandem Nenitzescu Reaction/Nucleophilic Aromatic Substitution to Form Novel Pyrido Fused Indole Frameworks - Singh - 2021 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/b05e09f8-6fc1-4702-a89a-af02fcc11394/ejoc202100827-toc-0001-m.jpg)
Tandem Nenitzescu Reaction/Nucleophilic Aromatic Substitution to Form Novel Pyrido Fused Indole Frameworks - Singh - 2021 - European Journal of Organic Chemistry - Wiley Online Library
![Design, synthesis, antitubercular and antiviral properties of new spirocyclic indole derivatives | SpringerLink Design, synthesis, antitubercular and antiviral properties of new spirocyclic indole derivatives | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00706-019-02457-9/MediaObjects/706_2019_2457_Figa_HTML.png)
Design, synthesis, antitubercular and antiviral properties of new spirocyclic indole derivatives | SpringerLink
![Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-022-09799-1/MediaObjects/41598_2022_9799_Fig6_HTML.png)
Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports
![Synthetic Methods for 3,4‐Fused Tricyclic Indoles via Indole Ring Formation - Nemoto - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library Synthetic Methods for 3,4‐Fused Tricyclic Indoles via Indole Ring Formation - Nemoto - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/3f87a0d3-8dab-4457-bf56-2a4cd14aa0e7/ajoc201800336-fig-5012-m.jpg)
Synthetic Methods for 3,4‐Fused Tricyclic Indoles via Indole Ring Formation - Nemoto - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library
![Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-022-09799-1/MediaObjects/41598_2022_9799_Fig2_HTML.png)
Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9 | Scientific Reports
![Synthetic Methods for 3,4‐Fused Tricyclic Indoles via Indole Ring Formation - Nemoto - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library Synthetic Methods for 3,4‐Fused Tricyclic Indoles via Indole Ring Formation - Nemoto - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/69babc6b-37ba-4c54-8e9f-66130b17082e/ajoc201800336-fig-5010-m.jpg)