RJ
Rahul A. Jagtap
The University of Tokyo, National Chemical Laboratory
Research areas: Chemistry · Organic Chemistry · Catalytic C–H Functionalization Methods · Catalytic Cross-Coupling Reactions · Crystal structures of chemical compounds
0000-0002-6253-5911
Employment
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The University of Tokyo JSPS Postdoctoral Researcher
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (15)
- Sustainable and Mild Catalytic Acceptorless Dehydrogenations Save
- An Efficient Route to 3,3′‐Biindolinylidene‐diones by Iron‐Catalyzed Dimerization of Isatins Save
- Nickel‐Catalyzed C−H Bond Functionalization of Azoles and Indoles Save
- Achiral and chiral NNN-pincer nickel complexes with oxazolinyl backbones: application in transfer hydrogenation of ketones Save
- Iron-Catalyzed C(sp2)–H Alkylation of Indolines and Benzo[h]quinoline with Unactivated Alkyl Chlorides through Chelation Assistance Save
- MnBr2-Catalyzed Direct and Site-Selective Alkylation of Indoles and Benzo[h]quinoline Save
- C−H Functionalization of Indoles by 3d Transition‐Metal Catalysis Save
- Corrigendum to: Expeditious and Solvent-Free Nickel-Catalyzed C−H Arylation of Arenes and Indoles(ChemSusChem, (2017), 10, (2242-2248), 10.1002/cssc.201700321) Save
- Scope and Mechanistic Aspect of Nickel-Catalyzed Alkenylation of Benzothiazoles and Related Azoles with Styryl Bromides Save
- Nickel-Catalyzed Straightforward and Regioselective C–H Alkenylation of Indoles with Alkenyl Bromides: Scope and Mechanistic Aspect Save
- Copper(I) complexes of ether- and thioether-based phosphines Save
- Copper(I) complexes of ether-and thioether-based phosphines Save
- Expeditious and Solvent-Free Nickel-Catalyzed C−H Arylation of Arenes and Indoles Save
- Unified Strategy for Nickel-Catalyzed C-2 Alkylation of Indoles through Chelation Assistance Save
- Mechanistic Insights into Pincer-Ligated Palladium-Catalyzed Arylation of Azoles with Aryl Iodides: Evidence of a PdII–PdIV–PdII Pathway Save