The cinnamate-based aminohalogenation provides an easy access to anti methyl 3-aryl-N-p-tosyl- and N-o-nosyl-aziridine-2-carboxylates
Author:
Publisher
ARKAT USA, Inc.
Subject
Organic Chemistry
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Non-Aziridination Approaches to 3-Arylaziridine-2-carboxylic Acid Derivatives and 3-Aryl-(aziridin-2-yl)ketones;International Journal of Molecular Sciences;2022-05-25
2. Regio- and Diastereoselective Vicinal Aminobromination of Electron Deficient Olefins via Phosphorus-Based GAP Protocol;Frontiers in Chemistry;2021-09-08
3. Highly diastereoselective aminobromination of β-methyl-β-nitrostyrenes with t-butyl N,N-dibromocarbamate/t-butyl carbamate as bromine/nitrogen sources;Tetrahedron Letters;2013-05
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5. A Rapid and Simple Method for Quantitative Aziridination from Aminobrominated Derivatives of Olefins under Solvent-free and Mild Conditions;Chinese Journal of Chemistry;2012-01-19
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