Synthesis of aziridines using new catalytic systems with bromamine-T as the nitrene source
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference11 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Development of the Copper-Catalyzed Olefin Aziridination Reaction
3. Bromamine-T: A superior source of nitrene for aziridination of olefins
4. Bis(oxazoline)-copper complexes as chiral catalysts for the enantioselective aziridination of olefins
5. Asymmetric alkene aziridination with readily available chiral diimine-based catalysts
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1. A Comparative Study of Cationic Copper(I) Reagents Supported by Bipodal Tetramethylguanidinyl-Containing Ligands as Nitrene-Transfer Catalysts;ACS Omega;2024-03-21
2. Cationic Divalent Metal Sites (M = Mn, Fe, Co) Operating as Both Nitrene-Transfer Agents and Lewis Acids toward Mediating the Synthesis of Three- and Five-MemberedN-Heterocycles;Inorganic Chemistry;2023-06-23
3. Bromamine-T (TsNBrNa): A Biologically Significant, Versatile Bromo-Organic Reagent;Synlett;2023-05-09
4. Fe(II)‐Catalyzed Synthesis of Unactivated Aziridines (N‐H/N‐Me) from Olefins Using O ‐Arylsulfonyl Hydroxylamines;ChemistrySelect;2021-10-14
5. Is the Electrophilicity of the Metal Nitrene the Sole Predictor of Metal-Mediated Nitrene Transfer to Olefins? Secondary Contributing Factors as Revealed by a Library of High-Spin Co(II) Reagents;Organometallics;2021-06-04
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