Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles **
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles ** ; day:02 ; month:06 ; year:2022 ; extent:1
Angewandte Chemie / International edition. International edition ; (02.06.2022) (gesamt 1)
- Creator
-
Sabat, Nazarii
Zhou, Weiping
Gandon, Vincent
Guinchard, Xavier
Vincent, Guillaume
- DOI
-
10.1002/anie.202204400
- URN
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urn:nbn:de:101:1-2022060315222903718490
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:27 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sabat, Nazarii
- Zhou, Weiping
- Gandon, Vincent
- Guinchard, Xavier
- Vincent, Guillaume
Other Objects (12)
Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles **
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On the Barton Copper‐Catalyzed C3‐Arylation of Indoles using Triarylbismuth bis (trifluoroacetate) Reagents
Electrophilic substitutions of indoles and pyrroles: : kinetics and synthetic applications
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Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles **
XtalFluor‐E Enabled Regioselective Synthesis of Di‐Indole Sulfides by C3−H Sulfenylation of Indoles
Indoles.
On the Barton Copper‐Catalyzed C3‐Arylation of Indoles using Triarylbismuth bis (trifluoroacetate) Reagents
Electrophilic substitutions of indoles and pyrroles: : kinetics and synthetic applications
Photocatalytic PPh 3 ‐Mediated Synthesis of C3‐Functionalized Indoles via Radical Annulation of Nitroarenes and Alkenes
Bench‐Stable Electrophilic Reagents for the Direct Di‐ and Trifluoroethylthiolation of Indoles
Book Review, Indoles
MnFe 2 O 4 Nanoparticles‐Catalyzed C3‐Alkylation of Indoles with Benzyl Alcohols under Solvent‐Free Conditions
C.3.
C3
[C3]
Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles **
XtalFluor‐E Enabled Regioselective Synthesis of Di‐Indole Sulfides by C3−H Sulfenylation of Indoles
Indoles.
On the Barton Copper‐Catalyzed C3‐Arylation of Indoles using Triarylbismuth bis (trifluoroacetate) Reagents
Electrophilic substitutions of indoles and pyrroles: : kinetics and synthetic applications
Photocatalytic PPh 3 ‐Mediated Synthesis of C3‐Functionalized Indoles via Radical Annulation of Nitroarenes and Alkenes
Bench‐Stable Electrophilic Reagents for the Direct Di‐ and Trifluoroethylthiolation of Indoles
Book Review, Indoles
MnFe 2 O 4 Nanoparticles‐Catalyzed C3‐Alkylation of Indoles with Benzyl Alcohols under Solvent‐Free Conditions
C.3.
C3