An Electrophilic Bromine Redox Catalysis for the Synthesis of Indole Alkaloid Building Blocks by Selective Aliphatic C−H Amination

Promoting Intermolecular C–N Bond Formation under the Auspices of Iodine(III)

(2018) Kilian Muñiz   ACCOUNTS OF CHEMICAL RESEARCH

Designing Homogeneous Bromine Redox Catalysis for Selective Aliphatic C−H Bond Functionalization

(2018) Peter Becker et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Iodine-Catalyzed C–H Amidation and Imination at the 2α-Position of 2,3-Disubstituted Indoles with Chloramine Salts

(2018) Xiaozu Liu et al.   JOURNAL OF ORGANIC CHEMISTRY

Directed Fischer Indolization as an Approach to the Total Syntheses of (+)-Aspidospermidine and (−)-Tabersonine

(2017) Joo-Young Kim et al.   ORGANIC LETTERS

Cyclohepta[b]indoles: A Privileged Structure Motif in Natural Products and Drug Design

(2016) Erik Stempel et al.   ACCOUNTS OF CHEMICAL RESEARCH

Synthesis and Structure of Hypervalent Iodine(III) Reagents Containing Phthalimidate and Application to Oxidative Amination Reactions

(2015) Kensuke Kiyokawa et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Regioselective C–H bond amination by aminoiodanes

(2015) Abhishek A. Kantak et al.   CHEMICAL COMMUNICATIONS

tert-Butyl hypochlorite mediated diastereoselective oxidative coupling: access to 1-functionalized tetrahydrocarbazoles

(2015) Long Jiang et al.   RSC Advances

Hypervalent Iodine(III)-Mediated Oxidative Decarboxylation of β,γ-Unsaturated Carboxylic Acids

(2014) Kensuke Kiyokawa et al.   ORGANIC LETTERS

Regioselective Gold-Catalyzed Oxidative C–N Bond Formation

(2014) Louis Marchetti et al.   ORGANIC LETTERS

The Witkop Cyclization: A Photoinduced CH Activation of the Indole System

(2013) Philipp J. Gritsch et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Enantioselective Palladium-Catalyzed Decarboxylative Allylation of Carbazolones: Total Synthesis of (−)-Aspidospermidine and (+)-Kopsihainanine A

(2013) Zeqian Li et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Aerobic C–H amination of tetrahydrocarbazole derivatives via photochemically generated hydroperoxides

(2013) Naeem Gulzar et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Metal-free catalytic vicinal diamination of alkenes

(2013) Kilian Muñiz   PURE AND APPLIED CHEMISTRY

Iodine in Modern Oxidation Catalysis

(2013) Boris Nachtsheim et al.   SYNTHESIS-STUTTGART

Is There No End to the Total Syntheses of Strychnine? Lessons Learned in Strategy and Tactics in Total Synthesis

(2012) Jeffrey S. Cannon et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Defined Hypervalent Iodine(III) Reagents Incorporating Transferable Nitrogen Groups: Nucleophilic Amination through Electrophilic Activation

(2012) José A. Souto et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Iodine-Mediated α-Acetoxylation of 2,3-Disubstituted Indoles

(2012) Hisaaki Zaimoku et al.   ORGANIC LETTERS

Hofmann-Type Rearrangement of Imides by in Situ Generation of Imide-Hypervalent Iodines(III) from Iodoarenes

(2012) Katsuhiko Moriyama et al.   ORGANIC LETTERS

Metal-free diamination of alkenes employing bromide catalysis

(2012) Patricia Chávez et al.   Chemical Science

Photochemical Reactions as Key Steps in Natural Product Synthesis

(2011) Thorsten Bach et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Catalysis with In Situ-Generated (Hypo)iodite Ions for Oxidative Coupling Reactions

(2011) Muhammet Uyanik et al.   ChemCatChem

Intermolecular Oxidative C–N Bond Formation under Metal-Free Conditions: Control of Chemoselectivity between Aryl sp2and Benzylic sp3C–H Bond Imidation

(2011) Hyun Jin Kim et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Metal-Free Intermolecular Oxidative C–N Bond Formation via Tandem C–H and N–H Bond Functionalization

(2011) Abhishek A. Kantak et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Utilization of N−X Bonds in The Synthesis of N-Heterocycles

(2009) Satoshi Minakata   ACCOUNTS OF CHEMICAL RESEARCH

Stereoselective aziridination of cyclic allylic alcohols using chloramine-T

(2008) Susannah C. Coote et al.   ORGANIC & BIOMOLECULAR CHEMISTRY