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Synthesis of 3-arylated indolines from dearomatization of indoles

Tetrahedron letters, 2015-07, Vol.56 (30), p.4413-4429

2015

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Regioselective Hydroarylation Reactions of C3 Electrophilic N-Acetylindoles Activated by FeCl3: An Entry to 3-(Hetero)arylindolines

Chemistry : a European journal, 2014-06, Vol.20 (24), p.7492-7500

2014

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Bioinspired Direct Access to Benzofuroindolines by Oxidative [3 + 2] Annulation of Phenols and Indoles

Organic letters, 2014-11, Vol.16 (21), p.5752-5755

2014

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Counteranion-Directed Catalysis in the Tsuji-Trost Reaction: Stereocontrolled Access to 2,5-Disubstituted 3-Hydroxy-Tetrahydrofurans

Angewandte Chemie International Edition, 2012-10, Vol.51 (42), p.10510-10514

International ed. in English, 2012

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Catalyst control over sixfold stereogenicity

Nature catalysis, 2021-06, Vol.4 (6), p.457-462

2021

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Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3

Chemical communications (Cambridge, England), 2016-01, Vol.52 (30), p.5328-5331

2016

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Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations

Angewandte Chemie International Edition, 2020-01, Vol.59 (3), p.1279-1285

International ed. in English, 2020

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Triflic Acid as an Efficient Brønsted Acid Promoter for the Umpolung of N‐Ac Indoles in Hydroarylation Reactions

Advanced synthesis & catalysis, 2018-01, Vol.360 (1), p.161-172

2018

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Enantioselective Cu-Catalyzed Arylation of Secondary Phosphine Oxides with Diaryliodonium Salts toward the Synthesis of P‑Chiral Phosphines

Journal of the American Chemical Society, 2016-10, Vol.138 (40), p.13183-13186

2016

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Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations

Angewandte Chemie, 2020-01, Vol.132 (3), p.1295-1301

2020

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FeCl3-Mediated Friedel-Crafts Hydroarylation with Electrophilic N-Acetyl Indoles for the Synthesis of Benzofuroindolines

Angewandte Chemie International Edition, 2012-12, Vol.51 (50), p.12546-12550

International ed. in English, 2012

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Hidden Heptacyclic Chiral N‐Acyl Iminium Ions: A New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid‐Promoted Intramolecular Pictet‐Spengler Reaction

Chemistry : a European journal, 2022-05, Vol.28 (25), p.e202200432-n/a

2022

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The Quest for an Oxidative Coupling of Phenols and Indoles towards Benzofuroindolines: A Two-Stage Approach

Synlett, 2014-12, Vol.26 (4), p.432-440

2014

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Revealing the electrophilicity of N-Ac indoles with FeCl3: a mechanistic study

Chemical communications (Cambridge, England), 2017-05, Vol.53 (43), p.5834-5837

2017

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Regioselective Hydroarylation Reactions of C3 Electrophilic N ‐Acetylindoles Activated by FeCl 3 : An Entry to 3‐(Hetero)arylindolines

Chemistry : a European journal, 2014-06, Vol.20 (24), p.7492-7500

2014

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Regioselective Hydroarylation Reactions of C3 Electrophilic N-Acetylindoles Activated by FeCl sub(3): An Entry to 3-(Hetero)arylindolines

Chemistry : a European journal, 2014-06, Vol.20 (24), p.7492-7500

2014

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Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3Electronic supplementary information (ESI) available: Experimental procedures, characterisation and NMR spectra of new compounds and X-ray data. CCDC 1450298-1450300. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6cc01654e

2016-04

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Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl sub(3)

Chemical communications (Cambridge, England), 2016-04, Vol.52 (30), p.5328-5331

2016

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Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl 3

Chemical communications (Cambridge, England), 2016, Vol.52 (30), p.5328-5331

2016

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Publisher Correction: Catalyst control over sixfold stereogenicity

Nature catalysis, 2021-06, Vol.4 (6), p.534-534

2021

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Revealing the electrophilicity of N-Ac indoles with FeCl3: a mechanistic studyElectronic supplementary information (ESI) available. CCDC 1535137 and 1535138. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7cc02756g

2017-05

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Revealing the electrophilicity of N-Ac indoles with FeCl 3 : a mechanistic study

Chemical communications (Cambridge, England), 2017-05, Vol.53 (43), p.5834-5837

2017

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FeCl 3 ‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N ‐Acetyl Indoles for the Synthesis of Benzofuroindolines

Angewandte Chemie International Edition, 2012-12, Vol.51 (50), p.12546-12550

2012

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Revealing the electrophilicity of N-Ac indoles with FeCl _\textrm3 : a mechanistic study

Chemical communications (Cambridge, England), 2017, Vol.53 (43), p.5834-5837

2017

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Counteranion-Directed Catalysis in the Tsuji-Trost Reaction: Stereocontrolled Access to 2,5-Disubstituted 3-Hydroxy-Tetrahydrofurans

Angewandte Chemie International Edition, 2012-10, Vol.51 (42), p.10510-10514

2012

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Synthesis of 3-arylated indolines from dearomatization of indoles

Regioselective Hydroarylation Reactions of C3 Electrophilic N-Acetylindoles Activated by FeCl3: An Entry to 3-(Hetero)arylindolines

Bioinspired Direct Access to Benzofuroindolines by Oxidative [3 + 2] Annulation of Phenols and Indoles

Counteranion-Directed Catalysis in the Tsuji-Trost Reaction: Stereocontrolled Access to 2,5-Disubstituted 3-Hydroxy-Tetrahydrofurans

Catalyst control over sixfold stereogenicity

Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3

Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations

Triflic Acid as an Efficient Brønsted Acid Promoter for the Umpolung of N‐Ac Indoles in Hydroarylation Reactions

Enantioselective Cu-Catalyzed Arylation of Secondary Phosphine Oxides with Diaryliodonium Salts toward the Synthesis of P‑Chiral Phosphines

Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations

FeCl3-Mediated Friedel-Crafts Hydroarylation with Electrophilic N-Acetyl Indoles for the Synthesis of Benzofuroindolines

Hidden Heptacyclic Chiral N‐Acyl Iminium Ions: A New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid‐Promoted Intramolecular Pictet‐Spengler Reaction

The Quest for an Oxidative Coupling of Phenols and Indoles towards Benzofuroindolines: A Two-Stage Approach

Revealing the electrophilicity of N-Ac indoles with FeCl3: a mechanistic study

Regioselective Hydroarylation Reactions of C3 Electrophilic N ‐Acetylindoles Activated by FeCl 3 : An Entry to 3‐(Hetero)arylindolines

Regioselective Hydroarylation Reactions of C3 Electrophilic N-Acetylindoles Activated by FeCl sub(3): An Entry to 3-(Hetero)arylindolines

Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl sub(3)

Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl 3

Publisher Correction: Catalyst control over sixfold stereogenicity

Revealing the electrophilicity of N-Ac indoles with FeCl3: a mechanistic studyElectronic supplementary information (ESI) available. CCDC 1535137 and 1535138. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7cc02756g

Revealing the electrophilicity of N-Ac indoles with FeCl 3 : a mechanistic study

FeCl 3 ‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N ‐Acetyl Indoles for the Synthesis of Benzofuroindolines

Revealing the electrophilicity of N-Ac indoles with FeCl _\textrm3 : a mechanistic study

Counteranion-Directed Catalysis in the Tsuji-Trost Reaction: Stereocontrolled Access to 2,5-Disubstituted 3-Hydroxy-Tetrahydrofurans

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