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Hentz, Alexandre, Retailleau, Pascal, Gandon, Vincent, Cariou, Kevin, Dodd, Robert H. (2014) Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angewandte Chemie, 126 (32). 8473-8477 doi:10.1002/ange.201402767

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Reference TypeJournal (article/letter/editorial)
TitleTransition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides
JournalAngewandte Chemie
AuthorsHentz, AlexandreAuthor
Retailleau, PascalAuthor
Gandon, VincentAuthor
Cariou, KevinAuthor
Dodd, Robert H.Author
Year2014 (August 4)Volume126
Issue32
PublisherWiley
DOIdoi:10.1002/ange.201402767Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID7325672Long-form Identifiermindat:1:5:7325672:2
GUID0
Full ReferenceHentz, Alexandre, Retailleau, Pascal, Gandon, Vincent, Cariou, Kevin, Dodd, Robert H. (2014) Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angewandte Chemie, 126 (32). 8473-8477 doi:10.1002/ange.201402767
Plain TextHentz, Alexandre, Retailleau, Pascal, Gandon, Vincent, Cariou, Kevin, Dodd, Robert H. (2014) Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angewandte Chemie, 126 (32). 8473-8477 doi:10.1002/ange.201402767
In(2014, August) Angewandte Chemie Vol. 126 (32) Wiley

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Hentz, Alexandre, Retailleau, Pascal, Gandon, Vincent, Cariou, Kevin, Dodd, Robert H. (2014) Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angewandte Chemie International Edition, 53 (32). 8333-8337 doi:10.1002/anie.201402767
Beaumont, Stéphane, Pons, Valérie, Retailleau, Pascal, Dodd, Robert H., Dauban, Philippe (2010) Catalytic Oxyamidation of Indoles. Angewandte Chemie, 122 (9). 1678-1681 doi:10.1002/ange.200906650
Grayfer, Tatyana D., Retailleau, Pascal, Dodd, Robert H., Dubois, Joëlle, Cariou, Kevin (2017) Chemodivergent, Tunable, and Selective Iodine(III)-Mediated Bromo-Functionalizations of Polyprenoids. Organic Letters, 19. 4766-4769 doi:10.1021/acs.orglett.7b02125
Beaumont, Stéphane, Pons, Valérie, Retailleau, Pascal, Dodd, Robert H., Dauban, Philippe (2010) Catalytic Oxyamidation of Indoles. Angewandte Chemie International Edition, 49 (9). 1634-1637 doi:10.1002/anie.200906650
Romero, Eugénie, Minard, Corinne, Benchekroun, Mohamed, Ventre, Sandrine, Retailleau, Pascal, Dodd, Robert H., Cariou, Kevin (2017) Base-Mediated Generation of Ketenimines from Ynamides: Direct Access to Azetidinimines by an Imino-Staudinger Synthesis. Chemistry - A European Journal, 23 (53). 12991-12994 doi:10.1002/chem.201702545
Sabat, Nazarii, Zhou, Weiping, Gandon, Vincent, Guinchard, Xavier, Vincent, Guillaume (2022) Unbiased C3‐Electrophilic Indoles: Triflic Acid Mediated C3‐Regioselective Hydroarylation of N−H Indoles**. Angewandte Chemie, 134 (30) doi:10.1002/ange.202204400
Nakanishi, Masafumi, Minard, Corinne, Retailleau, Pascal, Cariou, Kevin, Dodd, Robert H. (2011) Copper(I) Catalyzed Regioselective Asymmetric Alkoxyamination of Aryl Enamide Derivatives. Organic Letters, 13. 5792-5795 doi:10.1021/ol202367d
Romero, Eugénie, Minard, Corinne, Benchekroun, Mohamed, Ventre, Sandrine, Retailleau, Pascal, Dodd, Robert H., Cariou, Kevin (2017) Cover Feature: Base-Mediated Generation of Ketenimines from Ynamides: Direct Access to Azetidinimines by an Imino-Staudinger Synthesis (Chem. Eur. J. 53/2017). Chemistry - A European Journal, 23 (53). 12956 doi:10.1002/chem.201703248
Nocquet-Thibault, Sophie, Retailleau, Pascal, Cariou, Kevin, Dodd, Robert H. (2013) Iodine(III)-Mediated Umpolung of Bromide Salts for the Ethoxybromination of Enamides. Organic Letters, 15. 1842-1845 doi:10.1021/ol400453b
Dodd, Robert H., Cariou, Kevin (2018) Frontispiece: Ketenimines Generated from Ynamides: Versatile Building Blocks for Nitrogen-Containing Scaffolds. Chemistry - A European Journal, 24 (10). doi:10.1002/chem.201881061
Mahe, Capucine, Blacque, Olivier, Gasser, Gilles, Gandon, Vincent, Cariou, Kevin (2023) N-Metallocenyl Ynamides: Preparation, Reactivity, and Synthesis of ansa[3]-Ferrocenylamides. Organic Letters, 25 (4) 624-629 doi:10.1021/acs.orglett.2c04169
 
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