# Synthesis of Indole Derivatives

**Type:** Topics  
**Canonical URL:** https://scholariq.org/topics/synthesis-of-indole-derivatives/

## Facts

| Field | Value |
| --- | --- |
| Description | This cluster of papers explores the chemistry of quinone methides, focusing on their use as reactive intermediates in organic synthesis, asymmetric catalysis, and natural product synthesis. The research covers a wide range of catalytic reactions, including enantioselective synthesis, aromatic alkylation, and spiroketal synthesis. |
| Domain | Physical Sciences |
| Field | Chemistry |
| OpenAlex ID | t12973 |
| Works | 10 |

## Topic papers all

- [Single-Dose and Multiple-Dose Administration of Indole-3-Carbinol to Women: Pharmacokinetics Based on 3,3′-Diindolylmethane](https://scholariq.org/papers/single-dose-and-multiple-dose-administration-of-indole-3-carbinol-to-women/)
- [Decarboxylative acylation of indolines with α-keto acids under palladium catalysis: a facile strategy for the synthesis of 7-substituted indoles](https://scholariq.org/papers/decarboxylative-acylation-of-indolines-with-keto-acids-under-palladium-catalysis/)
- [Bioactive Bis-naphtho-γ-pyrones from Rice False Smut Pathogen <i>Ustilaginoidea virens</i>](https://scholariq.org/papers/bioactive-bis-naphtho-pyrones-from-rice-false-smut-pathogen-i-ustilaginoidea/)
- [Enantioselective Organocatalytic 1,6-Addition of Azlactones to <i>para</i>-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters](https://scholariq.org/papers/enantioselective-organocatalytic-1-6-addition-of-azlactones-to-i-para-i-quinone/)
- [Synthesis of tetraketones in water and under catalyst-free conditions](https://scholariq.org/papers/synthesis-of-tetraketones-in-water-and-under-catalyst-free-conditions/)
- [An Efficient Friedel–Crafts/Oxa‐Michael/Aromatic Annulation: Rapid Access to Substituted Naphtho\[2,1‐<i>b</i>\]furan, Naphtho\[1,2‐<i>b</i>\]furan, and Benzofuran Derivatives](https://scholariq.org/papers/an-efficient-friedel-crafts-oxa-michael-aromatic-annulation-rapid-access-to/)
- [One‐Pot Synthesis of Highly Fluorescent Pyrido\[1,2‐<i>a</i>\]indole Derivatives through CH/NH Activation: Photophysical Investigations and Application in Cell Imaging](https://scholariq.org/papers/one-pot-synthesis-of-highly-fluorescent-pyrido-1-2-i-a-i-indole-derivatives/)
- [Green synthesis of biscoumarin derivatives catalyzed by recyclable CuO–CeO2 nanocomposite catalyst in water](https://scholariq.org/papers/green-synthesis-of-biscoumarin-derivatives-catalyzed-by-recyclable-cuo-ceo2/)
- [Matrine Reduces Proliferation of Human Lung Cancer Cells by Inducing Apoptosis and Changing miRNA Expression Profiles](https://scholariq.org/papers/matrine-reduces-proliferation-of-human-lung-cancer-cells-by-inducing-apoptosis/)
- [Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from <i>N</i><sup>1</sup>‐Alkyne‐1,2‐diamines](https://scholariq.org/papers/diversity-oriented-synthesis-of-indoloazepinobenzimidazole-and/)

## Topic primary papers

- [Single-Dose and Multiple-Dose Administration of Indole-3-Carbinol to Women: Pharmacokinetics Based on 3,3′-Diindolylmethane](https://scholariq.org/papers/single-dose-and-multiple-dose-administration-of-indole-3-carbinol-to-women/)
- [Bioactive Bis-naphtho-γ-pyrones from Rice False Smut Pathogen <i>Ustilaginoidea virens</i>](https://scholariq.org/papers/bioactive-bis-naphtho-pyrones-from-rice-false-smut-pathogen-i-ustilaginoidea/)
- [Enantioselective Organocatalytic 1,6-Addition of Azlactones to <i>para</i>-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters](https://scholariq.org/papers/enantioselective-organocatalytic-1-6-addition-of-azlactones-to-i-para-i-quinone/)
- [An Efficient Friedel–Crafts/Oxa‐Michael/Aromatic Annulation: Rapid Access to Substituted Naphtho\[2,1‐<i>b</i>\]furan, Naphtho\[1,2‐<i>b</i>\]furan, and Benzofuran Derivatives](https://scholariq.org/papers/an-efficient-friedel-crafts-oxa-michael-aromatic-annulation-rapid-access-to/)

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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.