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Corrigendum: Expeditious and Solvent‐Free Nickel‐Catalyzed C−H Arylation of Arenes and Indoles

ChemSusChem, 2020-11, Vol.13 (21), p.5771-5771

2020

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Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields

Chemical reviews, 2014-05, Vol.114 (9), p.5057-5115

2014

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Electrochemical Dearomatization of Indoles: Access to Diversified Fluorine-Containing Spirocyclic Indolines

Organic letters, 2022-04, Vol.24 (15), p.2788-2792

2022

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Total Synthesis of Rucaparib

Journal of organic chemistry, 2022-04, Vol.87 (7), p.4813-4817

2022

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Stereodivergent assembly of tetrahydro-γ-carbolines via synergistic catalytic asymmetric cascade reaction

Nature communications, 2019-12, Vol.10 (1), p.5553-11, Article 5553

2019

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Synthesis of Spirocyclic Indolenines

Chemistry : a European journal, 2016-02, Vol.22 (9), p.2856-2881

2016

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Indole: A privileged scaffold for the design of anti-cancer agents

European journal of medicinal chemistry, 2019-12, Vol.183, p.111691-111691, Article 111691

2019

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Three-component synthesis of arylsulfonyl-substituted indolo[2,1- a ]isoquinolinones and benzimidazo-[2,1- a ]isoquinolin-6(5 H )-ones by SO 2 insertion and radical cascade cyclization

Organic & biomolecular chemistry, 2022-04, Vol.20 (15), p.3067-3071

2022

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Diels‐Alder Cycloaddition of Azepinoindoles Towards Hydrocarbazole Derivatives and Related Heterocycles

Advanced synthesis & catalysis, 2022-02, Vol.364 (4), p.873-889

2022

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Indole in the target-based design of anticancer agents: A versatile scaffold with diverse mechanisms

European journal of medicinal chemistry, 2018-04, Vol.150, p.9-29

2018

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A review on recent developments of indole-containing antiviral agents

European journal of medicinal chemistry, 2015-01, Vol.89, p.421-441

2015

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Nintedanib: From Discovery to the Clinic

Journal of medicinal chemistry, 2015-02, Vol.58 (3), p.1053-1063

2015

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Isolation and Antibacterial Activity of Indole Alkaloids from Pseudomonas aeruginosa UWI-1

Molecules (Basel, Switzerland), 2020-08, Vol.25 (16), p.3744

2020

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Biomedical importance of indoles

Molecules, 2013-06, Vol.18 (6), p.6620-6662

2013

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Discovery and Preclinical Characterization of 6‑Chloro-5-[4-(1-hydroxycyclobutyl)phenyl]‑1H‑indole-3-carboxylic Acid (PF-06409577), a Direct Activator of Adenosine Monophosphate-activated Protein Kinase (AMPK), for the Potential Treatment of Diabetic Nephropathy

Journal of medicinal chemistry, 2016-09, Vol.59 (17), p.8068-8081

2016

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Construction of sulfur-containing moieties in the total synthesis of natural products

Natural product reports, 2020-02, Vol.37 (2), p.246-275

2020

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Synthetic Approaches to 3‑(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds

Chemical reviews, 2014-07, Vol.114 (14), p.7108-7149

2014

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Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

European journal of medicinal chemistry, 2017-07, Vol.134, p.159-184

2017

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An insight into the medicinal perspective of synthetic analogs of indole: A review

European journal of medicinal chemistry, 2019-10, Vol.180, p.562-612

2019

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Arbidol as a broad-spectrum antiviral: An update

Antiviral research, 2014-07, Vol.107, p.84-94

2014

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Standard first-line chemotherapy with or without nintedanib for advanced ovarian cancer (AGO-OVAR 12): a randomised, double-blind, placebo-controlled phase 3 trial

The lancet oncology, 2016, Vol.17 (1), p.78-89

2016

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Correction: Tandem Prins cyclization for the synthesis of indole fused spiro-1,4-diazocane scaffolds

Organic & biomolecular chemistry, 2020-09, Vol.18 (36), p.7224-7224

2020

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Indole-fused azepines and analogues as anticancer lead molecules: Privileged findings and future directions

European journal of medicinal chemistry, 2017-12, Vol.142, p.244-265

2017

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Recent Advances towards the Synthesis and Material Applications of Indoloindoles

Chemistry, an Asian journal, 2022-08, Vol.17 (16), p.e202200460-n/a

2022

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Toxic indole alkaloids avrainvillamide and stephacidin B produced by a biocide tolerant indoor mold Aspergillus westerdijkiae

Toxicon (Oxford), 2015-06, Vol.99, p.58-67

2015

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Corrigendum: Expeditious and Solvent‐Free Nickel‐Catalyzed C−H Arylation of Arenes and Indoles

Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields

Electrochemical Dearomatization of Indoles: Access to Diversified Fluorine-Containing Spirocyclic Indolines

Total Synthesis of Rucaparib

Stereodivergent assembly of tetrahydro-γ-carbolines via synergistic catalytic asymmetric cascade reaction

Synthesis of Spirocyclic Indolenines

Indole: A privileged scaffold for the design of anti-cancer agents

Three-component synthesis of arylsulfonyl-substituted indolo[2,1- a ]isoquinolinones and benzimidazo-[2,1- a ]isoquinolin-6(5 H )-ones by SO 2 insertion and radical cascade cyclization

Diels‐Alder Cycloaddition of Azepinoindoles Towards Hydrocarbazole Derivatives and Related Heterocycles

Indole in the target-based design of anticancer agents: A versatile scaffold with diverse mechanisms

A review on recent developments of indole-containing antiviral agents

Nintedanib: From Discovery to the Clinic

Isolation and Antibacterial Activity of Indole Alkaloids from Pseudomonas aeruginosa UWI-1

Biomedical importance of indoles

Discovery and Preclinical Characterization of 6‑Chloro-5-[4-(1-hydroxycyclobutyl)phenyl]‑1H‑indole-3-carboxylic Acid (PF-06409577), a Direct Activator of Adenosine Monophosphate-activated Protein Kinase (AMPK), for the Potential Treatment of Diabetic Nephropathy

Construction of sulfur-containing moieties in the total synthesis of natural products

Synthetic Approaches to 3‑(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

An insight into the medicinal perspective of synthetic analogs of indole: A review

Arbidol as a broad-spectrum antiviral: An update

Standard first-line chemotherapy with or without nintedanib for advanced ovarian cancer (AGO-OVAR 12): a randomised, double-blind, placebo-controlled phase 3 trial

Correction: Tandem Prins cyclization for the synthesis of indole fused spiro-1,4-diazocane scaffolds

Indole-fused azepines and analogues as anticancer lead molecules: Privileged findings and future directions

Recent Advances towards the Synthesis and Material Applications of Indoloindoles

Toxic indole alkaloids avrainvillamide and stephacidin B produced by a biocide tolerant indoor mold Aspergillus westerdijkiae

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